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The increasing use of smartphones offers unprecedented opportunities for data collection. We developed a free smartphone application to assess fluctuations of patients' well-being as a result of surgical treatment and possible AEs. The application is installed on each patient's smartphone and collects standardized data... |
By acquiring longitudinal patient-reported outcome before and after neurosurgical interventions, we aim to determine the regular postoperative course for specific surgical procedures, as well as any deviation thereof, depending on the occurrence and severity of AEs. We will evaluate the validity of existing AE classifi... |
<|newrecord|> nctId: NCT06352697 id: DELI_MASLD briefTitle: Probiotic Lysate (Postbiotic and Metabiotic) Supplementation for Adults MASLD Patients (DELI_MASLD Study) overallStatus: COMPLETED date: 2023-02-01 date: 2023-12-31 date: 2023-12-31 date: 2024-04-08 date: 2024-04-09 name: Bogomolets National Medical University... |
The study will include 3 periods. Screening period of up to 1 weeks to assess the eligibility to inclusion/exclusion criteria. Treatment period for 3 month where the participants will receive a twice daily oral dose of postbiotics (cell lysate and DNA fragments of the probiotic strain L. rhamnosus DV - NRRLB-68023) at ... |
<|newrecord|> nctId: NCT06352684 id: DP0001-SEV-CAB-II id: RS-2023-00227526 type: OTHER_GRANT domain: Korea Ministry of Science and ICT briefTitle: Multi-Reader Multi-Case, Retrospective Study to Evaluate Effectiveness of CadAI-B for Breast overallStatus: ACTIVE_NOT_RECRUITING date: 2023-11-24 date: 2025-01-14 date: 20... |
<|newrecord|> nctId: NCT06352671 id: 023-286 briefTitle: Prospective Long-Term Outcomes of a Standardized Ross Procedure acronym: ROSS overallStatus: RECRUITING date: 2023-10-12 date: 2025-12-01 date: 2026-01-01 date: 2024-04-08 date: 2024-04-08 name: Baylor Research Institute class: OTHER briefSummary: This standardiz... |
<|newrecord|> nctId: NCT06352658 id: #1/2024 briefTitle: Efficacy of Mandibular Advancement Device for Mild-Moderate Apnea overallStatus: COMPLETED date: 2023-02-01 date: 2024-01-01 date: 2024-01-10 date: 2024-04-08 date: 2024-04-08 name: Nourhan M.Aly class: OTHER briefSummary: This was a prospective randomized contro... |
<|newrecord|> nctId: NCT06352645 id: STUDY00004879 briefTitle: Evaluation of Safety and Efficacy of Bixdo Ultra Compact Water Flosser overallStatus: NOT_YET_RECRUITING date: 2024-05-01 date: 2025-05-01 date: 2026-05-01 date: 2024-04-08 date: 2024-04-09 name: Tufts University class: OTHER name: Guangdong Bixdo Health Te... |
<|newrecord|> nctId: NCT06352632 id: ACT-GLOBAL_Master briefTitle: A Multi-faCtorial, mulTi-arm, Multi-staGe, Randomised, gLOBal Adaptive pLatform Trial for Stroke acronym: ACT-GLOBAL overallStatus: NOT_YET_RECRUITING date: 2024-04 date: 2024-04 date: 2034-04 date: 2024-04-08 date: 2024-04-23 name: The George Institute... |
<|newrecord|> nctId: NCT06352619 id: ACT-GLOBAL_AIS_03 briefTitle: Third Enhanced Control of Hypertension and Thrombectomy Stroke Domain Within ACT-GLOBAL Adaptive Platform Trial acronym: ENCHANTED3/MT overallStatus: NOT_YET_RECRUITING date: 2024-04 date: 2026-04 date: 2026-04 date: 2024-04-08 date: 2024-04-23 name: Th... |
<|newrecord|> nctId: NCT06352606 id: 36264PR558/2/24 briefTitle: Spinal and General Anesthesia in Neonates Undergoing Herniorrhaphy overallStatus: RECRUITING date: 2024-04-06 date: 2024-09-01 date: 2024-09-01 date: 2024-04-08 date: 2024-04-09 name: Tanta University class: OTHER briefSummary: The aim of this study is to... |
<|newrecord|> nctId: NCT06352593 id: 36264PR557/2/24 briefTitle: Intraoperative Dexmedetomidine Infusion in Endovascular Intervention for Aneurysmal Subarachnoid Hemorrhage overallStatus: RECRUITING date: 2024-04-06 date: 2024-09-01 date: 2024-09-01 date: 2024-04-08 date: 2024-04-09 name: Tanta University class: OTHER ... |
<|newrecord|> nctId: NCT06352580 id: COVID-19 Pediatric briefTitle: Covid-19 Pandemic and Pediatric Dentistry overallStatus: COMPLETED date: 2022-03-01 date: 2022-06-30 date: 2022-06-30 date: 2024-04-08 date: 2024-04-08 name: Abant Izzet Baysal University class: OTHER briefSummary: Coronavirus (SARS-CoV-2), which emerg... |
<|newrecord|> nctId: NCT06352567 id: BakircayU1394/1414 briefTitle: Symptoms Associated With Chemotherapy-Induced Peripheral Neuropathy overallStatus: RECRUITING date: 2024-01-18 date: 2024-06-22 date: 2024-08 date: 2024-04-08 date: 2024-04-09 name: Izmir Bakircay University class: OTHER briefSummary: Breast cancer rem... |
<|newrecord|> nctId: NCT06352554 id: 2023/ETH02474:STING id: 224842/Z/21/Z type: OTHER_GRANT domain: Wellcome Trust id: 75A50122C00028 type: OTHER_GRANT domain: HHS/BARDA OTA briefTitle: Susceptibility Testing In Neisseria Gonorrhoeae (STING) Study, Assessing the Performance of a New Rapid Test for Gonorrhoea Antibioti... |
The hypothesis is that the InSignia test will be able to detect transcriptional responses after incubation in antibiotic for susceptible strains and not resistant strains. |
Furthermore, this study will also add to our understanding on the performance of this test in various clinical specimens. conditions: Diagnosis conditions: Gonorrhea conditions: Resistance Bacterial studyType: OBSERVATIONAL observationalModel: COHORT timePerspective: CROSS_SECTIONAL count: 100 type: ESTIMATED measure: ... |
<|newrecord|> nctId: NCT06352541 id: SOPH232-1122/I briefTitle: Study Evaluating PRO-232 an Ophthalmic Solution Compared to Placebo. acronym: PRO-232 overallStatus: NOT_YET_RECRUITING date: 2024-05-30 date: 2025-06-30 date: 2025-06-30 date: 2024-04-08 date: 2024-04-11 name: Laboratorios Sophia S.A de C.V. class: INDUST... |
<|newrecord|> nctId: NCT06352528 id: CA127-1070 briefTitle: A Study to Assess the Drug Levels of Repotrectinib in Healthy Participants and Participants With Moderate and Severe Hepatic Impairment overallStatus: NOT_YET_RECRUITING date: 2024-04-26 date: 2025-07-24 date: 2025-07-24 date: 2024-04-08 date: 2024-04-08 name:... |
<|newrecord|> nctId: NCT06352515 id: T cells in Ulcerative colitis briefTitle: T Lymphocyte Subsets in Ulcerative Colitis overallStatus: NOT_YET_RECRUITING date: 2024-06-01 date: 2026-06-01 date: 2027-06-01 date: 2024-04-08 date: 2024-04-29 name: Assiut University class: OTHER briefSummary: 1. Study the distribution of... |
2. Correlation of T-cell subsets to therapeutic response/ disease activity. |
3. Assess the value of circulating IgG anti-Integrin αvβ6 in UC. conditions: Ulcerative Colitis studyType: OBSERVATIONAL observationalModel: CASE_CONTROL timePerspective: RETROSPECTIVE count: 80 type: ESTIMATED name: Flow cytometry measure: Study the distribution of T-cell subsets among ulcerative colitis patients. mea... |
<|newrecord|> nctId: NCT06352502 id: 202112-28 briefTitle: An Observational Study of Furmonertinib for EGFR Mutation-positive NSCLC Patients With Brain Metastasis overallStatus: RECRUITING date: 2022-01-28 date: 2024-09-30 date: 2024-09-30 date: 2024-04-08 date: 2024-04-08 name: Tang-Du Hospital class: OTHER briefSumma... |
<|newrecord|> nctId: NCT06352489 id: Posterior component separation briefTitle: Evaluation of Posterior Component Separation Technique in the Management of Complex Ventral Hernia. overallStatus: NOT_YET_RECRUITING date: 2024-05-01 date: 2026-05 date: 2026-06 date: 2024-04-08 date: 2024-04-08 name: Assiut University cla... |
* Detect most common post operative complications related to AWR techniques in a 6 months duration after operation. conditions: Ventral Hernia studyType: INTERVENTIONAL phases: NA allocation: RANDOMIZED interventionModel: PARALLEL primaryPurpose: TREATMENT masking: NONE count: 30 type: ESTIMATED name: Posterior compone... |
<|newrecord|> nctId: NCT06352476 id: 10881-669 briefTitle: The Effect of Sleep Hygiene Given to Epilepsy Patients on Seizure Frequency and Sleep Quality overallStatus: ACTIVE_NOT_RECRUITING date: 2023-06-01 date: 2024-12-01 date: 2024-12-01 date: 2024-04-08 date: 2024-04-08 name: Marmara University class: OTHER briefSu... |
Purpose of the research; To determine the effect of sleep hygiene training given to epilepsy patients on seizure frequency and sleep quality. Non-drug clinical research is an experimentally planned research with a pre-test post-test control group trial model. conditions: Epilepsy studyType: INTERVENTIONAL phases: NA al... |
<|newrecord|> nctId: NCT06352463 id: 406.XS.03.068 briefTitle: Intervention Social Anxiety: Combining Parent-child Treatment acronym: ISA overallStatus: RECRUITING date: 2024-04-15 date: 2025-07-01 date: 2025-07-01 date: 2024-04-08 date: 2024-04-08 name: Leiden University class: OTHER name: Leids Universitair Behandel ... |
<|newrecord|> nctId: NCT06352450 id: DPT/Batch-Fall19/558 briefTitle: Comparison of Active Isolated Stretching Versus Myofascial Release of Knee Joint in Office Workers overallStatus: ACTIVE_NOT_RECRUITING date: 2024-01-15 date: 2024-05-20 date: 2024-06-28 date: 2024-04-08 date: 2024-04-08 name: Superior University cla... |
AIS involves stretching specific muscles while actively engaging opposing muscles to enhance the effectiveness of the stretch. It aims to increase the extensibility of muscles and improve joint mobility. On the other hand, MFR focuses on releasing tension and adhesions in the fascia, the connective tissue surrounding m... |
Understanding the benefits and effectiveness of these techniques will contribute to evidence-based practices in occupational health and help office workers maintain optimal joint health" conditions: Stiffness; Spine conditions: Mobility Limitation studyType: INTERVENTIONAL phases: NA allocation: RANDOMIZED intervention... |
<|newrecord|> nctId: NCT06352437 id: 1507-0001 id: 2023-508767-79-00 type: REGISTRY domain: CTIS id: U1111-1302-5933 type: REGISTRY domain: WHO International Clinical Trials Registry Platform (ICTRP) briefTitle: A Study to Test How Well Different Doses of BI 3034701 Are Tolerated by Healthy Men and People With Overweig... |
The purpose of this study is to find out how well different doses of BI 3034701 are tolerated by healthy men (Part A) and people with overweight or obesity (Part B). Another goal of this study is to find out how different doses of BI 3034701 are taken up in the blood. |
Participants get different doses of BI 3034701 or placebo as an injection under the skin. In Part A, every participant gets a single dose. In Part B, every participant gets several doses of BI 3034701 or placebo. In this study, BI 3034701 is given to humans for the first time. |
Participants in Part A are in the study up to 10 weeks. During this time, they visit the study site 8 times. Participants in Part B are in the study for about 6 months. They visit the study regularly. At some of the visits, participants in both parts stay at the study site for up to 5 nights. During the study, the doct... |
<|newrecord|> nctId: NCT06352424 id: 1458-0006 id: 2023-506233-30-01 type: REGISTRY domain: CTIS (EU) id: U1111-1293-4672 type: REGISTRY domain: WHO Registry briefTitle: A Study in People With Overweight or Obesity to Test How BI 1820237, BI 456906, or a Combination of Both Affects Brain Activity overallStatus: NOT_YET... |
<|newrecord|> nctId: NCT06352411 id: 1404-0009 id: 2023-508557-13-00 type: REGISTRY domain: CTIS id: U1111-1298-3135 type: REGISTRY domain: WHO registry briefTitle: A Study to Test How BI 456906 is Taken up in the Blood of People With and Without Kidney Problems overallStatus: NOT_YET_RECRUITING date: 2024-05-08 date: ... |
The purpose of this study is to find out how much of a medicine called BI 456906 gets into the blood of people with and without kidney problems. BI 456906 is being developed to treat people with obesity and liver problems. People living with these conditions often also have kidney problems. Therefore, it is important t... |
Study participants receive a single dose of BI 456906 as an injection under the skin. Participants are divided into 4 groups based on how well their kidneys work: 1 group without kidney problems, and 3 groups with mild, moderate, and severe kidney problems. Each participant without kidney problems is matched with parti... |
Participants are in the study for about 2 months. They stay for 5 days and 4 nights at the study site and visit their doctors about 7 times. During these visits, the doctors collect information about participants' health. To assess the study endpoints, the doctors regularly take blood samples from the participants. The... |
<|newrecord|> nctId: NCT06352398 id: BBTuysuz briefTitle: Comparison of Analgesic Efficacy in Video-Assisted Thoracoscopic Surgery Patients overallStatus: COMPLETED date: 2023-12-20 date: 2024-02-01 date: 2024-04-01 date: 2024-04-08 date: 2024-04-08 name: Burcu Bozdogan Tuysuz class: OTHER briefSummary: The 52 patients... |
<|newrecord|> nctId: NCT06352385 id: SH9H-2024-TK16-1.0 briefTitle: Epidemiological Investigation of Malocclusion in China overallStatus: NOT_YET_RECRUITING date: 2024-04 date: 2026-12 date: 2026-12 date: 2024-04-08 date: 2024-04-08 name: Shanghai Jiao Tong University School of Medicine class: OTHER briefSummary: Maloc... |
<|newrecord|> nctId: NCT06352372 id: tPBM Study briefTitle: Safety and Efficacy of tPBM for Epileptiform Activity in Autism acronym: tPBM overallStatus: NOT_YET_RECRUITING date: 2024-04 date: 2025-04 date: 2025-06 date: 2024-04-08 date: 2024-04-08 name: Richard Frye class: OTHER briefSummary: For this study, the propos... |
<|newrecord|> nctId: NCT06352359 id: ONC-841-002 briefTitle: Safety, Pharmacokinetics (PK), and Efficacy of ONC 841 in Advanced Solid Tumors overallStatus: NOT_YET_RECRUITING date: 2024-06-30 date: 2025-06-30 date: 2027-06-30 date: 2024-04-08 date: 2024-04-10 name: OncoC4, Inc. class: INDUSTRY briefSummary: This is a P... |
<|newrecord|> nctId: NCT06352346 id: Plan Game_ABI&Psychiatry briefTitle: A Single-case Design to Investigate a Compensatory Brain Game Supporting Goal Management Training Intervention in a Psychiatric Brain Injury Population overallStatus: NOT_YET_RECRUITING date: 2024-05 date: 2025-12 date: 2025-12 date: 2024-04-08 d... |
Phase A acts as a control and is therefore compared with phase B. primaryPurpose: TREATMENT masking: SINGLE maskingDescription: The target behavior (i.e. performance on an untrained shopping task) will be measured repeatedly, on a minimum of six occasions in each phase where possible, in accordance with the recommendat... |
<|newrecord|> nctId: NCT06352333 id: Parasagittal Vs Cornerpocket briefTitle: Parasagittal Vs Cornerpocket Approaches overallStatus: NOT_YET_RECRUITING date: 2024-04-02 date: 2024-11-01 date: 2025-01-01 date: 2024-04-08 date: 2024-04-08 name: Sohag University class: OTHER briefSummary: Brachial plexus blocks are widely... |
Although many different approaches to the brachial plexus block have been described, there is widespread acceptance that injecting at the supraclavicular level is the most reliable method in terms of spread of local anesthetic agent. |
Each approach of ultrasound guided supraclavicular brachial plexus block (US -SCBPB ) has a different success rate and complications. . |
A supraclavicular block can provide effective surgical anesthesia of the forearm and hand. |
The most commonly performed US- SCBPB is the corner pocket approach which was described by Chan et al with probe resting posterior to the clavicle, with postero latero-anteromedial orientation provides a very stable location, but has the disadvantage of "looking" across the first rib, with the apex of the lung visualiz... |
A new Parasagittal approach for brachial plexus block at the supraclavicular level was studied by Adrian Searle where the arc of the first rib was used to provide a deep limit to needle transit in order to minimize the risk of pneumothorax ;the aim of our study is to further evaluate the parasagittal approach for brach... |
* 18to60 yearsold |
* ASA grade I to II |
* Elective upper limb surgery primaryPurpose: SCREENING masking: NONE count: 80 type: ESTIMATED name: supraclavicular ultrasound guided brachial plexus block measure: Needle visibility in both approaches measure: Duration of sensory and motor block measure: Success rate measure: Complications sex: ALL minimumAge: 18 Ye... |
<|newrecord|> nctId: NCT06352320 id: XJTU1AF2023LSK-533 briefTitle: Risk Stratification and New Early Prevention and Treatment Strategies for Patients With Cardiomyopathy (STRENGTH） overallStatus: NOT_YET_RECRUITING date: 2024-12-31 date: 2030-08-31 date: 2032-08-31 date: 2024-04-08 date: 2024-04-08 name: First Affilia... |
<|newrecord|> nctId: NCT06352307 id: XJTU1AF2023LSK-532 briefTitle: Risk Stratification, Early Prevention and Treatment Strategies for Arrhythmogenic Cardiomyopathy acronym: STARTER overallStatus: NOT_YET_RECRUITING date: 2024-12-31 date: 2030-08-31 date: 2032-08-31 date: 2024-04-08 date: 2024-04-08 name: First Affilia... |
<|newrecord|> nctId: NCT06352294 id: MSDALAKCI briefTitle: The Effects of Myofascial Relaxation Technique Applied Together With Core Stabilization Trainings on Balance, Pain, Joint Range of Motion and Functionality in Individuals With Chronic Neck Pain overallStatus: RECRUITING date: 2024-03-29 date: 2024-07 date: 2024... |
Postural control is based on the process of correctly identifying and selectively focusing the incoming afferent input of the Central Nervous System (CNS). |
The main treatment options for people with neck pain include soft tissue and joint mobilizations, stabilization exercises for the neck, trunk and shoulder muscles, cervical Deckings, relaxation training, strengthening exercises and body awareness and posture training Nov. |
In this study, it was aimed to investigate the effects of myofascial relaxation on balance, pain, joint range of motion and functionality in individuals with chronic neck pain by dividing them into two groups in the form of core stabilization and core stabilization and myofascial relaxation. |
The study included 45 people between the ages of 18 and 65 Dec. In two groups, the core stabilization group will be 22 people, and the core stabilization and myofascial relaxation group will be 23 people. The study period is planned as 6 weeks and 3 sessions per week. conditions: Neck Pain studyType: INTERVENTIONAL pha... |
<|newrecord|> nctId: NCT06352281 id: KM-007 briefTitle: Efficacy and Safety of CAR-T Cells Therepy for Chronic or Refractory Primary Immune Thrombocytopenia (ITP) overallStatus: RECRUITING date: 2024-02-01 date: 2026-01-01 date: 2027-12-31 date: 2024-04-08 date: 2024-04-08 name: 920th Hospital of Joint Logistics Suppor... |
<|newrecord|> nctId: NCT06352268 id: IEC-368/17.07.2023 briefTitle: Lesioning Procedures for Movement Disorders overallStatus: NOT_YET_RECRUITING date: 2024-04-15 date: 2027-12-31 date: 2028-12-31 date: 2024-04-08 date: 2024-04-08 name: All India Institute of Medical Sciences, New Delhi class: OTHER briefSummary: Dysto... |
<|newrecord|> nctId: NCT06352255 id: AR1937 briefTitle: Pain and Anxiety During Local Block overallStatus: NOT_YET_RECRUITING date: 2024-07 date: 2024-12 date: 2025-07 date: 2024-04-08 date: 2024-04-08 name: University of Seville class: OTHER briefSummary: INTRODUCTION: Currently, there is no scientific evidence about ... |
OBJECTIVES: It is intended to determine the pain after an anesthetic block in H of Frost in the first finger with different application methods, such as syringe and carpule. As secondary objectives, it is intended to establish the difference in pain according to the sex and age of the patients. |
METHODOLOGY: Experimental, transverse and random clinical trial type analytical study, in which a sample of 200 individuals will be selected, 100 per group, which would require digital anesthesia of the first finger and that would fulfill the inclusion criteria. |
Result: after the completion of the study CONCLUSIONS: After the completion of the study conditions: Anesthesia, Local conditions: Pain conditions: Anxiety studyType: INTERVENTIONAL phases: NA allocation: RANDOMIZED interventionModel: CROSSOVER primaryPurpose: OTHER masking: DOUBLE whoMasked: PARTICIPANT whoMasked: INV... |
<|newrecord|> nctId: NCT06352242 id: RECHMPL24-0076 UF 9572 briefTitle: Is Trogocytosis a Predictive Marker of CAR-T Cell Response in Diffuse Large B-cell Lymphoma? acronym: CARTROG overallStatus: NOT_YET_RECRUITING date: 2024-04-08 date: 2026-04-08 date: 2026-04-08 date: 2024-04-08 date: 2024-04-08 name: University Ho... |
<|newrecord|> nctId: NCT06352229 id: 514-0335/23-2000 briefTitle: The Playful Learning in Infancy Program acronym: PLIP overallStatus: RECRUITING date: 2023-06-01 date: 2026-11-30 date: 2026-11-30 date: 2024-04-08 date: 2024-04-08 name: University of Copenhagen class: OTHER name: LEGO Foundation briefSummary: In the Pl... |
The aims of the Playful Learning in Infancy Program are to 1) promote playful interactions between infants and parents, parental attitudes towards play, and infant socioemotional development; 2) enhance the language and knowledge of playful learning in infancy among frontline staff; and 3) evaluate the Playful Learning... |
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