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<|newrecord|> nctId: NCT06361654 id: 2023/0135/OB briefTitle: Effect of Muscular Imbalance Between Flexors and Extensors of the Fingers and Wrist on Upper Limb Injuries in Climbers acronym: CRIMPER overallStatus: RECRUITING date: 2024-03-25 date: 2025-03-25 date: 2025-09-01 date: 2024-04-12 date: 2024-04-15 name: Unive... |
The study will be carried out on club-licensed climbers, as they are better supervised. They will be recruited through requests sent to various clubs. The measurements will be taken during different climbing sessions, after the warm-up. |
The study will include measurements on different climbers. Informed consent and personal data will be collected from the climbers before the measurements are taken. The strength values of the flexors and extensors of the fingers and wrist will be measured using a dynamometer. The climbers will then continue their usual... |
<|newrecord|> nctId: NCT06361641 id: 49RC23_0259 id: AO2721-44 type: OTHER domain: ANSM briefTitle: Functional and Phenotypic Characterization of Monocytes in Myeloproliferative Syndromes acronym: PHEMOP overallStatus: NOT_YET_RECRUITING date: 2024-04-20 date: 2025-10-19 date: 2027-10-19 date: 2024-04-12 date: 2024-04-... |
<|newrecord|> nctId: NCT06361628 id: RIVER-EU WP4 briefTitle: Implementation and Evaluation of Tailored Interventions to Increase MMR and/or HPV Vaccine acronym: RIVER-EU overallStatus: NOT_YET_RECRUITING date: 2024-05-01 date: 2025-06-01 date: 2025-06-01 date: 2024-04-12 date: 2024-04-17 name: University Medical Cente... |
The main research question is: to what extent is the multicomponent tailored intervention effective to increase MMR/HPV intention and vaccine uptake in the target population in Greece, Netherlands, Poland and Slovakia? conditions: Vaccination conditions: Health Systems conditions: Knowledge, Attitudes, Practice studyTy... |
<|newrecord|> nctId: NCT06361615 id: CEC_FP_2023042 briefTitle: Effect of a Dual-task Intervention Program on Physical and Cognitive Function overallStatus: ACTIVE_NOT_RECRUITING date: 2023-11-08 date: 2024-03-05 date: 2024-04-05 date: 2024-04-12 date: 2024-04-12 name: University of Americas class: OTHER briefSummary: ... |
Methods: Participants were assigned randomly into two groups, ST (multicomponent physical exercise) and DT training (multicomponent physical exercise + cognitive tasks). Both groups performed the exercise three times per week for 1 month. Short Physical Performance Battery (SPPB), handgrip strength, Barthel Index and M... |
<|newrecord|> nctId: NCT06361602 id: SYSKY-2023-1015-01 briefTitle: Exploring the Effectiveness and Factors Affecting the Collection of Single Nucleated Cells From Different Volunteers acronym: SYX-AN-01 overallStatus: NOT_YET_RECRUITING date: 2024-05-01 date: 2027-05-01 date: 2027-05-01 date: 2024-04-12 date: 2024-04-... |
2. The data obtained will provide a reference for the MNC threshold for the subsequent clinical trials of immunocell therapy in hospitals. |
3. From the screening of volunteers, PBMC collection and transportation conditions and other specific details of the operation, risk assessment and the establishment of a safe operation standard process, for the hospital to carry out subsequent clinical trials of immune cell therapy to provide an effective reference. c... |
<|newrecord|> nctId: NCT06361589 id: EK2023003-1 briefTitle: Real World Study of Lolatinib for Advanced ALK+ NSCLC Patients overallStatus: RECRUITING date: 2024-05-01 date: 2026-11-01 date: 2028-11-01 date: 2024-04-12 date: 2024-04-12 name: Sichuan Cancer Hospital and Research Institute class: OTHER briefSummary: This ... |
<|newrecord|> nctId: NCT06361576 id: CA209-1443 briefTitle: Real-World Use of Nivolumab for the Treatment of Patients With Metastatic Upper Gastrointestinal Cancer in Canada overallStatus: COMPLETED date: 2023-09-05 date: 2024-01-25 date: 2024-01-25 date: 2024-04-12 date: 2024-04-12 name: Bristol-Myers Squibb class: IN... |
<|newrecord|> nctId: NCT06361563 id: CA209-1442 briefTitle: Real-World Use of Adjuvant Nivolumab in Patients With Upper Gastrointestinal Cancer in Canada overallStatus: COMPLETED date: 2023-09-05 date: 2024-01-25 date: 2024-01-25 date: 2024-04-12 date: 2024-04-12 name: Bristol-Myers Squibb class: INDUSTRY briefSummary:... |
<|newrecord|> nctId: NCT06361550 id: AYTO_SALAMANCA_001 briefTitle: Nutritional Status Assessment and Dietary Recommendations Program (VENREDI) overallStatus: RECRUITING date: 2023-11-02 date: 2025-06-30 date: 2025-12-30 date: 2024-04-12 date: 2024-04-12 name: University of Salamanca class: OTHER name: Ayuntamiento de ... |
Objective: To evaluate the effect of a multifactorial intervention (seminar on shopping basket and food labeling, workshop on healthy cooking and subsequent tasting of the prepared products) in improving adherence to the Mediterranean diet in older adults. |
Methodology: Randomized controlled clinical trial with two parallel groups: an intervention group (IG) and a control group (CG). The study population will be adults over 60 years of age, retired or pre-retired. A sample size of 200 participants has been estimated, 100 in each group to detect a difference of 0.83 points... |
All participants will receive an educational talk on healthy nutrition, with an estimated duration of 2 hours. The GI, in addition to this educational workshop, will receive a practical seminar on how to properly carry out the shopping cart. This will take place both in a market and later in a supermarket in Salamanca.... |
An initial and post-intervention evaluation will be carried out after 3 months so that both groups can study the change variables related to Adherence to the Mediterranean Diet \[Mediterranean Diet Adherence Questionnaire (MEDAS)\], physical activity \[Short physical performance battery (SPPB)\], sleep quality (ATENAS ... |
<|newrecord|> nctId: NCT06361537 id: CONE-02 briefTitle: Phase 3 Study of IV Human Plasma-derived C1 Esterase Inhibitor Concentrate in Patients With Congenital C1-INH Deficiency for Treatment and Pre-procedure Preventing of Acute Hereditary Angioedema Attacks overallStatus: NOT_YET_RECRUITING date: 2024-04 date: 2025-1... |
<|newrecord|> nctId: NCT06361524 id: 44967 id: 5F32HL143916 type: NIH link: https://reporter.nih.gov/quickSearch/5F32HL143916 id: 856341 type: OTHER_GRANT domain: American Heart Association briefTitle: Gut Microbiome Profiling in Patients With Chronic Heart Failure overallStatus: ENROLLING_BY_INVITATION date: 2018-08-0... |
1. How does the gut microbiome and its interactions with the host change over time in adults with chronic heart failure? |
2. How do these changes relate to heart failure disease severity and complications? conditions: Heart Failure With Reduced Ejection Fraction conditions: Nonischemic Cardiomyopathy studyType: OBSERVATIONAL observationalModel: COHORT timePerspective: PROSPECTIVE count: 150 type: ESTIMATED measure: Advanced heart failure-... |
<|newrecord|> nctId: NCT06361511 id: 2023H0284 briefTitle: The Foods & Oil to Repair, Correct and Enhance Strength (FORCES) Study overallStatus: NOT_YET_RECRUITING date: 2024-05-01 date: 2029-05-01 date: 2030-05-01 date: 2024-04-12 date: 2024-04-12 name: Ohio State University class: OTHER name: National Institutes of H... |
<|newrecord|> nctId: NCT06361498 id: 23-3115 briefTitle: Ultrasound for Evaluation of Percutaneous G-tube Position overallStatus: NOT_YET_RECRUITING date: 2024-04 date: 2025-03 date: 2025-03 date: 2024-04-12 date: 2024-04-12 name: University of North Carolina, Chapel Hill class: OTHER briefSummary: The goal of this cli... |
The main questions it aims to answer are: |
* If ultrasound is just as accurate as fluoroscopy to assess the GT position. |
* If ultrasound takes less time than fluoroscopy to assessing the GT position. |
Participants will be imaging using ultrasound to assess GT positioning before their standard of care fluoroscopic imaging. conditions: Gastrostomy studyType: INTERVENTIONAL phases: NA allocation: NA interventionModel: SINGLE_GROUP primaryPurpose: OTHER masking: NONE count: 10 type: ESTIMATED name: Ultrasound Imaging me... |
<|newrecord|> nctId: NCT06361485 id: 011624 briefTitle: Safety and Feasibility of Umbilical Cord Wharton's Jelly Allograft Injections for Lumbar Pain overallStatus: RECRUITING date: 2024-03-25 date: 2027-03-31 date: 2028-04-01 date: 2024-04-11 date: 2024-04-11 name: R3 Stem Cell class: INDUSTRY name: R3 Medical Researc... |
<|newrecord|> nctId: NCT06361472 id: 11695 briefTitle: Contextual Factors-Enriched Standard Care on Mechanical Neck Pain overallStatus: NOT_YET_RECRUITING date: 2024-05-01 date: 2025-08-31 date: 2025-11-30 date: 2024-04-11 date: 2024-04-15 name: Universidad Nacional de la Matanza class: OTHER briefSummary: The primary ... |
This will be an assessor-blinded, 2-group (1:1) randomized clinical trial aiming to enroll 94 participants with neck pain persisting for more than 4 weeks. Both groups will undergo 4 weeks of standard care twice weekly, following established clinical practice guidelines. In the intervention group, CFs will be enhanced,... |
The primary outcomes will encompass changes in Pain and Disability after 4 weeks of treatment, with a follow-up reassessment at week 12 post-treatment. Secondary outcomes will include changes in Active Range of Motion, Global Rating of Change, and Satisfaction with treatment. The change between groups after treatment a... |
<|newrecord|> nctId: NCT06361459 id: NL83858.058.12 briefTitle: Stop Smoking in Spine Surgery overallStatus: RECRUITING date: 2023-07-06 date: 2026-06-30 date: 2026-12-31 date: 2024-04-11 date: 2024-04-11 name: Leiden University Medical Center class: OTHER name: Medical Center Haaglanden name: Haga Hospital name: Alrij... |
<|newrecord|> nctId: NCT06361446 id: 023098816 briefTitle: Zonisamide Versus Propranolol in Migraine overallStatus: RECRUITING date: 2024-03-29 date: 2025-03-30 date: 2025-04-20 date: 2024-04-11 date: 2024-04-23 name: Kafrelsheikh University class: OTHER briefSummary: Investigators aim to compare the effect of zonisami... |
<|newrecord|> nctId: NCT06361433 id: R5-11 briefTitle: Intracerebral Transplantation of Autologous MSC Combined With Scaffold Product for Chronic Intracerebral Hemorrhage acronym: RAINBOW-Hx overallStatus: RECRUITING date: 2023-12-01 date: 2026-02 date: 2026-02 date: 2024-04-11 date: 2024-04-11 name: Hokkaido Universit... |
* The safety of the product |
* The efficacy of the product conditions: Intracerebral Hemorrhage studyType: INTERVENTIONAL phases: PHASE1 phases: PHASE2 allocation: NA interventionModel: SINGLE_GROUP primaryPurpose: TREATMENT masking: NONE count: 8 type: ESTIMATED name: HUFF-01 measure: Number of participants with treatment-related adverse events a... |
<|newrecord|> nctId: NCT06361420 id: 2023YF051-01 briefTitle: Driving Pressure-guided Lung Protective Ventilation acronym: DPV overallStatus: RECRUITING date: 2024-01-26 date: 2024-12-30 date: 2025-03-31 date: 2024-04-11 date: 2024-04-11 name: Yong Lin, PhD class: OTHER briefSummary: The study, named as "The Efficacy o... |
<|newrecord|> nctId: NCT06361407 id: 2023-A02464-41 briefTitle: Sensory and Cognitive Predictions, and Their Disruptions in Schizophrenia acronym: SensoSchiz overallStatus: NOT_YET_RECRUITING date: 2024-05-01 date: 2027-04-30 date: 2028-02-28 date: 2024-04-11 date: 2024-04-11 name: Centre Psychothérapique de Nancy clas... |
<|newrecord|> nctId: NCT06361394 id: CORPFIN0021 briefTitle: The Impacts of Mindfulness on Psychological Wellbeing Among Nursing Students overallStatus: RECRUITING date: 2024-02-20 date: 2024-07-25 date: 2025-08-31 date: 2024-04-11 date: 2024-04-11 name: Chang Gung University of Science and Technology class: OTHER brie... |
<|newrecord|> nctId: NCT06361381 id: 24-01-281 briefTitle: The Combined Effect of TENS and TaVNS on Pressure and Heat Pain Thresholds in Pain-Free Subjects overallStatus: NOT_YET_RECRUITING date: 2024-04 date: 2024-06 date: 2024-12 date: 2024-04-11 date: 2024-04-11 name: University of Hartford class: OTHER briefSummary... |
The study will be a simple crossover design conducted at the University of Hartford. Subjects will be recruited from the University of Hartford population via oral communication, digital flyers, and posters on campus. Thirty participants will undergo two sessions in a crossover manner with one week in between. During o... |
<|newrecord|> nctId: NCT06361368 id: NYCU112174AF briefTitle: Efficacy Assessment of Probiotics in Improving Sleep Indices overallStatus: NOT_YET_RECRUITING date: 2024-04 date: 2026-03 date: 2026-03 date: 2024-04-11 date: 2024-04-11 name: National Yang Ming University class: OTHER name: Bened Biomedical Co., Ltd. brief... |
<|newrecord|> nctId: NCT06361355 id: CMAB807-I-002 briefTitle: Study of CMAB807 Post-change in Manufacturing Site and Prolia in Healthy Volunteers overallStatus: RECRUITING date: 2023-11-02 date: 2024-04 date: 2024-06 date: 2024-04-11 date: 2024-04-11 name: Taizhou Mabtech Pharmaceutical Co.,Ltd class: INDUSTRY briefSu... |
<|newrecord|> nctId: NCT06361342 id: 23-003633 briefTitle: Smartphones Aggravating Anxiety Symptoms overallStatus: ENROLLING_BY_INVITATION date: 2024-03-08 date: 2025-03 date: 2025-03 date: 2024-04-11 date: 2024-04-11 name: Mayo Clinic class: OTHER briefSummary: The goal of this study is to assess if excessive use of s... |
<|newrecord|> nctId: NCT06361329 id: 20240030C briefTitle: Comparing the Efficacy of VHAG and Traditional Chemotherapy Regimens in Newly Diagnosed ETP-ALL overallStatus: RECRUITING date: 2024-04 date: 2026-03-31 date: 2027-03-31 date: 2024-04-11 date: 2024-04-29 name: First Affiliated Hospital of Zhejiang University cl... |
<|newrecord|> nctId: NCT06361316 id: CSPC-DEY-PC-JS01 briefTitle: Irinotecan Liposome Combined With Oxaliplatin and Tegafur as Adjuvant Therapy for Pancreatic Cancer overallStatus: RECRUITING date: 2024-04-08 date: 2025-03-25 date: 2028-07-31 date: 2024-04-11 date: 2024-04-11 name: Kuirong Jiang class: OTHER name: CSPC... |
<|newrecord|> nctId: NCT06361303 id: PS230001 id: PS230001 / PSS001 type: OTHER domain: US FDA briefTitle: The Happiest Baby, Inc. SNOO Postmarket Surveillance Study overallStatus: RECRUITING date: 2023-11-29 date: 2025-09 date: 2025-09 date: 2024-04-11 date: 2024-04-11 name: Happiest Baby, Inc. class: INDUSTRY briefSu... |
<|newrecord|> nctId: NCT06361290 id: APHP231703 briefTitle: Diaphyseal Reconstruction of Malignant Tumors in Children acronym: RDTM overallStatus: NOT_YET_RECRUITING date: 2024-04 date: 2024-10 date: 2024-10 date: 2024-04-11 date: 2024-04-11 name: Assistance Publique - Hôpitaux de Paris class: OTHER briefSummary: Prima... |
The objective of oncological resection is local control of the disease. Excision of the entire tumor should make it possible to maintain good function of the limb, minimizing morbidity, and promoting acceptance by the patient. |
Biological reconstructions offer the best long-term functional results. Several possibilities are then available: the Induced Membrane technique, the Vascularized Fibula and Vascularized Fibula associated with an Allograft. |
Until today, no reconstruction technique in children has proven its superiority over another and no decision-making algorithm for therapeutic care has been determined based on the importance of the bone resection and the affected segment in diaphyseal tumor reconstruction surgery of the lower limb. |
The aim of the present research is to compare the three techniques concerning the consolidation aspect, the reoperation rates, the rates of bone complications, septic, and the functional results by the study of the medical files of approximately 90 patients operated between 1986 and 2017. conditions: Childhood Malignan... |
<|newrecord|> nctId: NCT06361277 id: JW22104 briefTitle: To Evaluate the Pharmacokinetic Characteristics and Safety in Healthy Volunteers overallStatus: COMPLETED date: 2023-11-03 date: 2023-11-20 date: 2023-11-27 date: 2024-04-11 date: 2024-04-11 name: JW Pharmaceutical class: INDUSTRY briefSummary: The objective is t... |
<|newrecord|> nctId: NCT06361264 id: Karanahan briefTitle: Clinical Study of Personalized Chemotherapy for Breast Cancer With Low Doses of Cyclophosphamide overallStatus: RECRUITING date: 2018-11-01 date: 2024-12-01 date: 2025-12-01 date: 2024-04-11 date: 2024-04-11 name: KARANAHAN class: OTHER briefSummary: The goal o... |
<|newrecord|> nctId: NCT06361251 id: CS5_10 briefTitle: Interventional, Monocentric, Double-blind Randomized Category 2b Study Evaluating the Evaluation of the Tolerance of Cyto-selective Difluoroethane-based Cryotherapy in the Treatment of Brown Spots (Solar and Senile Lentigines, Post -Inflammatory Hyperpigmentation ... |
* the tolerance of 2 prototypes of cyto-selective cryotherapy treatments |
* the performance of 2 prototypes of cyto-selective cryotherapy treatments Participants will be treated for each spots with a definied prototype during 6 treatment visits. |
Researchers will compare the tolerance and performance of the 3 prototypes. conditions: Lentigo conditions: Solar Lentigo conditions: Post Inflammatory Hyperpigmentation studyType: INTERVENTIONAL phases: NA allocation: RANDOMIZED interventionModel: PARALLEL interventionModelDescription: Proof of concept study concernin... |
<|newrecord|> nctId: NCT06361238 id: 2023-LCYJ-PY-21 briefTitle: Liraglutide in Preventing Delirium in Diabetic Elderly After Cardiac Surgery overallStatus: NOT_YET_RECRUITING date: 2024-04-30 date: 2026-03-31 date: 2027-03-31 date: 2024-04-11 date: 2024-04-11 name: The Affiliated Nanjing Drum Tower Hospital of Nanjing... |
<|newrecord|> nctId: NCT06361225 id: 0075-24-MMC briefTitle: Routine Use of RUSH Protocol in the Intensive Care Unit overallStatus: NOT_YET_RECRUITING date: 2024-08-01 date: 2025-08-01 date: 2025-08-01 date: 2024-04-11 date: 2024-04-11 name: Meir Medical Center class: OTHER briefSummary: The RUSH protocol has been used... |
We would like to investigate whether the routine use of the RUSH protocol as part of the daily patient evaluation in the general intensive care unit will lead to any change in the patient's management. conditions: RUSH Protocol studyType: OBSERVATIONAL observationalModel: CASE_ONLY timePerspective: PROSPECTIVE count: 5... |
<|newrecord|> nctId: NCT06361212 id: BJXH-2022-002 briefTitle: Ethoximod Pharmacokinetics In Healthy Subjects overallStatus: COMPLETED date: 2022-09-01 date: 2022-09-20 date: 2024-01-12 date: 2024-04-11 date: 2024-04-11 name: Longevity Inc. class: INDUSTRY briefSummary: The goal of this clinical trial is to evaluate th... |
1. to evaluate the safety and tolerance of Ethoximod in healthy subjects after single or repeated doses. |
2. to assess the pharmacokinetics and pharmacodynamics of Ethoximod in healthy subjects after single or repeated doses. |
3. to evaluate of the effect of food on the pharmacokinetics of Ethoximod in healthy subjects Participants will receive test tablets or placebo at the indicated date and collect blood samples. conditions: Psoriasis studyType: INTERVENTIONAL phases: PHASE1 allocation: RANDOMIZED interventionModel: PARALLEL primaryPurpos... |
<|newrecord|> nctId: NCT06361199 id: BJXH-2021-001 briefTitle: Proximod Pharmacokinetics in Healthy Subjects and Patients With Rheumatoid Arthritis overallStatus: COMPLETED date: 2021-12-16 date: 2022-02-16 date: 2023-10-08 date: 2024-04-11 date: 2024-04-19 name: Longevity Inc. class: INDUSTRY briefSummary: The goal of... |
1. to evaluate the safety and tolerance of Proximod in health subjects after repeated doses. |
2. to assess the pharmacokinetics and pharmacodynamics of Proximod in healthy subjects after repeated doses. |
3. to evaluate the safety and tolerance of Proximod in patients with rheumatoid arthritis. |
4. to evaluate the pharmacokinetics and pharmacodynamics of Proximod in patients with rheumatoid arthritis. |
Participants will receive test tablets or placebo at the indicated date and collect blood samples. conditions: Rheumatoid Arthritis studyType: INTERVENTIONAL phases: PHASE1 allocation: RANDOMIZED interventionModel: PARALLEL primaryPurpose: TREATMENT masking: DOUBLE whoMasked: PARTICIPANT whoMasked: INVESTIGATOR count: ... |
<|newrecord|> nctId: NCT06361186 id: BJXH-2017-001 briefTitle: Proximod Pharmacokinetics In Healthy Subjects overallStatus: COMPLETED date: 2017-09-14 date: 2017-11-01 date: 2021-06-22 date: 2024-04-11 date: 2024-04-11 name: Longevity Inc. class: INDUSTRY briefSummary: The goal of this clinical trial is to evaluate the... |
1. to evaluate the safety and tolerance of Proximod in healthy subjects after single or repeated doses. |
2. to learn the pharmacodynamics of Proximod in healthy subjects after single or repeated doses. |
3. to evaluation of the effect of food on the pharmacokinetics of Proximod in healthy subjects Participants will receive test tablets or placebo at the indicated date and collect blood samples. conditions: Rheumatoid Arthritis studyType: INTERVENTIONAL phases: PHASE1 allocation: RANDOMIZED interventionModel: PARALLEL p... |
<|newrecord|> nctId: NCT06361173 id: STUDY00004127 briefTitle: Spanish BMT4me Usability & Acceptability overallStatus: NOT_YET_RECRUITING date: 2024-06-01 date: 2026-05-01 date: 2026-05-01 date: 2024-04-11 date: 2024-04-11 name: Nationwide Children's Hospital class: OTHER name: Columbia University briefSummary: The obj... |
<|newrecord|> nctId: NCT06361160 id: D23-P037 briefTitle: Reduction of Auditory-Verbal Hallucinations in Schizophrenia Through Cortical Neuromodulation acronym: HALLUSTIM overallStatus: NOT_YET_RECRUITING date: 2024-04 date: 2026-04 date: 2026-04 date: 2024-04-11 date: 2024-04-11 name: Centre Hospitalier St Anne class:... |
The research project comprises two phases: |
-Phase 1: randomized controlled clinical trial (1 weekly session per patient over 12 weeks: 6 active stimulation sessions and 6 sham sessions) evaluating the phasic effects of rTMS on AVHs as they appear during the sessions. |
Phase 2: open-label study offering patients a routine rTMS protocol which has demonstrated its effects on AVH (10 TMS sessions over one workweek - twice daily with 1-hour intervals, MULTIMODHAL study, NCT01373866). conditions: Treatment Resistant Schizophrenia studyType: INTERVENTIONAL phases: NA allocation: RANDOMIZED... |
<|newrecord|> nctId: NCT06361147 id: 3764/2-10-2019 briefTitle: Psychoeducation of Adult Siblings of ASD People (Autism Spectrum Disorder). overallStatus: ACTIVE_NOT_RECRUITING date: 2024-03-28 date: 2024-07 date: 2024-10 date: 2024-04-11 date: 2024-04-11 name: Hellenic Mediterranean University class: OTHER briefSummar... |
The psycho-educational program will be implemented in adult siblings of people with ASD and its effectiveness will be assessed. |
Participation in this program is expected to contribute in the improvement of the quality of life of the participants, their siblings with ASD and those related to them. No risk is identified. conditions: Autism Spectrum Disorder conditions: Sibling Relations studyType: INTERVENTIONAL phases: NA allocation: RANDOMIZED ... |
<|newrecord|> nctId: NCT06361134 id: 14574941-302,08,01- briefTitle: Efficacy of Supporting SAFE Early Intervention overallStatus: COMPLETED date: 2021-01-15 date: 2022-05-15 date: 2022-11-15 date: 2024-04-11 date: 2024-04-11 name: Gazi University class: OTHER briefSummary: Within the scope of the study, it was planned... |
<|newrecord|> nctId: NCT06361121 id: D361 briefTitle: Mid-point Transverse Process to Pleura Block Versus Thoracic Paravertebral Block in Posterolateral Thoracotomy overallStatus: RECRUITING date: 2024-03-01 date: 2025-03 date: 2025-03 date: 2024-04-11 date: 2024-04-11 name: Fayoum University Hospital class: OTHER brie... |
Costach et al introduced the mid-point transverse process to pleura block (MTP) as a modification of conventional paravertebral block by placing the LA posterior to the (SCTL) under ultrasound guidence achieving an effective block without the necessity to approach the pleura and the attendant risks. |
In recent studies ,the ultrasound guided MTP block provided an effective analgesia in various surgical procedures including mastectomy , video-assisted thoracic surgeries and cardiac surgeries. |
In our study we hypothesized that the mid-point transverse process to pleura (MTP) block can provide an effective analgesia comparable with thoracic paravertebral (TPV) block in adult patients undergoing posterolateral thoracotomy incisions. conditions: Bronchiectasis conditions: Lung Neoplasm conditions: Emphysematous... |
<|newrecord|> nctId: NCT06361108 id: YJ001-103 briefTitle: Multiple-Ascending Dose Study to Assess the Safety, Tolerability, Pharmacokinetics and Efficacy of YJ001 for Spray Use in Patients With Diabetic Peripheral Neuropathic Pain overallStatus: NOT_YET_RECRUITING date: 2024-04-10 date: 2025-03-20 date: 2025-03-20 dat... |
In this study, 2 cohorts (N=24, 12 subjects for each cohort), each cohort will consist of 10 active and 2 placebo, with approximately equal numbers of male and female subjects. |
Each subject will be administered a single dose of YJ001 as multiple sprays topically on both feet and below the ankle in the morning on Day 1 and Day 2, and will be administered as twice daily doses once in the morning and the other in the evening (with an interval of 11 to 13 h) from Day 3 through Day 11. conditions:... |
The Safety Review Committee (SRC), comprised of the Principal Investigator, Medical Monitor, and Sponsor's qualified designee, will convene after completion of each cohort to evaluate available safety, PK, and other relevant data. |
The SRC will determine whether to proceed to the next planned dose level, continue with the study and add additional safety evaluations, expand the number of subjects at the current level, reduce the dose, or stop the study. whoMasked: PARTICIPANT whoMasked: CARE_PROVIDER whoMasked: INVESTIGATOR whoMasked: OUTCOMES_ASS... |
<|newrecord|> nctId: NCT06361095 id: R01GABM briefTitle: Confirmatory Efficacy Trial of Attention Bias Modification for Depression overallStatus: NOT_YET_RECRUITING date: 2024-05-01 date: 2028-03-01 date: 2028-03-01 date: 2024-04-11 date: 2024-04-16 name: University of Texas at Austin class: OTHER name: Arcade Therapeu... |
* Aim 1:examine whether gamified ABM leads to greater change in the primary and secondary outcomes than sham ABM |
* Aim 1: establish that gamified ABM is at least as effective as traditional ABM. |
* Aim 2: identify moderators of ABM efficacy and mechanisms responsible for its efficacy. |
* Aim 3: Identify the durability of ABM on depression symptoms during short-term follow-up |
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