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Participants will: |
* complete baseline clinical measures |
* complete neuroimaging tasks via Functional Magnetic Resonance Imaging (fMR) |
* undergo a 12-session course of FFT-CD |
* complete follow up evaluations and neuroimaging conditions: Childhood Depression studyType: INTERVENTIONAL phases: NA allocation: NA interventionModel: SINGLE_GROUP primaryPurpose: TREATMENT masking: NONE count: 80 type: ESTIMATED name: Family-Focused Treatment for Childhood-Depression (FFT-CD) measure: Depression Tr... |
<|newrecord|> nctId: NCT06288997 id: TFYuan_tACS briefTitle: tACS Intervention for Methamphetamine Addiction acronym: tACS for MUD overallStatus: COMPLETED date: 2021-11-21 date: 2023-05-09 date: 2023-11-09 date: 2024-03-01 date: 2024-03-01 name: Shanghai Mental Health Center class: OTHER briefSummary: A growing body o... |
<|newrecord|> nctId: NCT06288984 id: NFEC-2024-061 briefTitle: Effects of rTMS on Respiratory Function and Gut Microbiota in Patients With Brain Injury overallStatus: NOT_YET_RECRUITING date: 2024-03-01 date: 2026-06-30 date: 2026-12-31 date: 2024-03-01 date: 2024-03-01 name: Nanfang Hospital, Southern Medical Universi... |
<|newrecord|> nctId: NCT06288971 id: IRCCS FSM briefTitle: Personalized Innovative Intervention Pathways to Promote EF in Children With CP overallStatus: NOT_YET_RECRUITING date: 2024-03-01 date: 2027-01-31 date: 2027-03-01 date: 2024-03-01 date: 2024-03-01 name: IRCCS Fondazione Stella Maris class: OTHER name: Univers... |
<|newrecord|> nctId: NCT06288958 id: Fondazione Stella Maris briefTitle: Quality of Life in Children With Cerebral Palsy overallStatus: COMPLETED date: 2019-04-01 date: 2020-12-31 date: 2021-12-31 date: 2024-03-01 date: 2024-03-01 name: IRCCS Fondazione Stella Maris class: OTHER briefSummary: Cerebral Palsy (CP) is an ... |
In order to best capture the peculiarities of CP, specific questionnaires were carried out to analyse the QOL in this clinical population. The Cerebral Palsy Quality of Life Questionnaire for Children (CP QOL-Child) is an internationally recognized CP-specific instrument based on the International Classification of Fun... |
The present study aims to deeper understand the perception of QOL and social participation in a group of Italian children with CP, as reported by their parents, using two commonly used questionnaires in the CP population (CP-QOL and PEM-CY). In addition, this study aims to explore the roles of specific clinical variabl... |
<|newrecord|> nctId: NCT06288945 id: Dry eye syndrome briefTitle: Effect of an Educational Program on Health-related Outcomes of Patients With Dry Eye Syndrome overallStatus: COMPLETED date: 2023-01-15 date: 2023-09-14 date: 2023-09-14 date: 2024-03-01 date: 2024-03-01 name: Alexandria University class: OTHER briefSumm... |
<|newrecord|> nctId: NCT06288932 id: NIBD/IRB-263/08-2023 briefTitle: Outcome Study of Conventional Steroids vs. Steroids Combined With Mycopehnolate in Newly Diagnosed Immune Thrombocytopenia Purpura. overallStatus: RECRUITING date: 2024-02 date: 2024-05 date: 2025-01 date: 2024-03-01 date: 2024-03-01 name: National I... |
<|newrecord|> nctId: NCT06288919 id: 2023-IMPLHYGIENE briefTitle: Erythritol vs Ultrasonic Scaler Prophylaxis Systems on Dental Implants With Crowns Made by Different Materials overallStatus: ENROLLING_BY_INVITATION date: 2024-03-01 date: 2026-04-01 date: 2026-04-10 date: 2024-03-01 date: 2024-04-26 name: University of... |
A randomized clinical trial will be conducted on the patient. Patients will be randomly divided into two groups: |
* Erythritol group: erythritol with a particle size of \~14 µm will be used for 5 seconds (AIRFLOW® PLUS EMS) |
* Ultrasonic scaler group: a piezoelectric handpiece with peek inserts (Mini Piezon EMS; PI EMS) will be used. |
Different subgroups will be defined according to the material of the dental crown of the related implant. |
The oral hygiene session will be carried out every 6 months (2-years follow-up; 6 sessions), after instruction and motivation of the patient, completion of the clinical chart with the recording of the Probing Depth (evaluation in mm of the peri-implant sulcus taken by a periodontal probe; 4 surfaces of the gingival mar... |
<|newrecord|> nctId: NCT06288906 id: ASTER Study briefTitle: Acute and Subacute Iliofemoral and/or Caval Deep Vein Thrombosis: Evaluation of Mechanical Thrombectomy Systems acronym: ASTER overallStatus: NOT_YET_RECRUITING date: 2024-03-30 date: 2027-03 date: 2027-12 date: 2024-03-01 date: 2024-03-04 name: IRCCS San Raf... |
<|newrecord|> nctId: NCT06288893 id: DEU-2001 briefTitle: SHEN211 Tablets for the Treatment of Mild and Moderate Novel Corona Virus Infections (COVID-19) overallStatus: NOT_YET_RECRUITING date: 2024-04-01 date: 2024-08-01 date: 2025-01-01 date: 2024-03-01 date: 2024-03-04 name: JKT Biopharma Co., Ltd. class: INDUSTRY b... |
<|newrecord|> nctId: NCT06288880 id: kilis_4 briefTitle: Impact of Earthquake Trauma on Nurses' Compassion Fatigue: A Study From Kahramanmaraş, Turkey overallStatus: NOT_YET_RECRUITING date: 2024-03-01 date: 2024-04-01 date: 2024-05-01 date: 2024-03-01 date: 2024-03-01 name: Kilis 7 Aralik University class: OTHER name:... |
<|newrecord|> nctId: NCT06288867 id: FMASU MD28/2024 briefTitle: A 12 Months Prospective Study Comparing Functional Outcome Scores in Hip Arthroscopic Labral Repair Versus Debridement overallStatus: NOT_YET_RECRUITING date: 2024-04-01 date: 2025-09-01 date: 2025-12-01 date: 2024-03-01 date: 2024-03-18 name: Ain Shams U... |
<|newrecord|> nctId: NCT06288854 id: 66222 briefTitle: Efficacy of Olanzapine on Weight Gain in Advanced Gynecologic Cancer With Paclitaxel and Carboplatin: a Double Blind, Placebo-controlled Randomized Trial overallStatus: NOT_YET_RECRUITING date: 2024-04-03 date: 2025-03-31 date: 2025-06-30 date: 2024-03-01 date: 202... |
* Proprotion of pateints in advanced stage gynecologic cancer who recieving paclitaxel and carboplatin chemotherapy gain weight on olanzapine or placebo conditions: Weight Gain studyType: INTERVENTIONAL phases: NA allocation: RANDOMIZED interventionModel: PARALLEL interventionModelDescription: olanzapine vs placebo pri... |
<|newrecord|> nctId: NCT06288841 id: TJMZ2023-008 briefTitle: Efficacy and Safety of Liposomal Bupivacaine Under ERAS Concept for Postoperative Analgesia of Ultrasound-Guided QLB in Gynecologic Laparoscopic Patients: A Randomized, Single-blind, Active-Controlled Clinical Study overallStatus: RECRUITING date: 2023-11-30... |
<|newrecord|> nctId: NCT06288828 id: IRB0569/66 briefTitle: The Efficacy of Aerobic Exercise Training on Autonomic Nervous System and Endothelial Function in Patients With Compensated Cirrhosis overallStatus: NOT_YET_RECRUITING date: 2024-03-05 date: 2024-08-01 date: 2025-12-31 date: 2024-03-01 date: 2024-03-01 name: K... |
1) What effect does 16 weeks of aerobic exercise have on changes in the autonomic nervous system and endothelial function in cirrhotic patients? |
Additionally, the secondary research questions are: |
1. How does a 16-week aerobic exercise program influence changes in muscle mass, muscle strength, and physical performance in cirrhotic patients? |
2. Is there a correlation between muscle mass and parameters of the autonomic nervous system in cirrhotic patients? |
Participants in the intervention group will undergo 150 minutes of moderate aerobic exercise per week for 16 weeks, accompanied by a personalized nutritional plan (1.2 grams of protein per kilogram of ideal body weight per day and a calorie intake of 35 kilocalories per kilogram of ideal body weight per day). The contr... |
<|newrecord|> nctId: NCT06288815 id: TUH oral fluid TKA briefTitle: Oral Fluid vs IV Fluid After Primary TKA overallStatus: RECRUITING date: 2024-01-10 date: 2024-12 date: 2025-06 date: 2024-03-01 date: 2024-03-04 name: Thammasat University Hospital class: OTHER briefSummary: The goal of this study is to compared effic... |
The main question it aims to answer is: |
Does oral fluid replacement after primary unilateral total knee arthroplasty provide a patient recover faster than intravenous fluids replacement? conditions: Osteoarthritis, Knee conditions: Total Knee Arthroplasty conditions: Oral Fluid Replacement studyType: INTERVENTIONAL phases: NA allocation: RANDOMIZED intervent... |
<|newrecord|> nctId: NCT06288802 id: 04-2023-200647 briefTitle: Study of Wilms Tumors Among Patients of Shefa Al-Orman Children Cancer Hospital overallStatus: RECRUITING date: 2020-06-15 date: 2024-06 date: 2024-12 date: 2024-03-01 date: 2024-03-01 name: South Egypt Cancer Institute class: OTHER name: Shefa Al-orman Ch... |
<|newrecord|> nctId: NCT06288789 id: SFI-TR briefTitle: Turkish Validity and Reliability of the Social Frailty Index overallStatus: COMPLETED date: 2024-02-25 date: 2024-03-20 date: 2024-03-30 date: 2024-03-01 date: 2024-04-25 name: Pamukkale University class: OTHER briefSummary: The aim was to examine the validity and... |
<|newrecord|> nctId: NCT06288776 id: SOD/ERB/2023/22-04 briefTitle: Efficacy of Azadirachta Indica Based Herbal Mouthwash in Treating the Tooth Hypersensitivity overallStatus: COMPLETED date: 2023-02-01 date: 2023-04-30 date: 2023-04-30 date: 2024-03-01 date: 2024-03-01 name: Pakistan Institute of Medical Sciences clas... |
Participants aged 20 years and above having Gingival Index score 3 will be included in the study. Their tooth sensitivity will be checked initially and then they will be given Herbal based mouthwash for 3 months. Again, their tooth sensitivity shall be checked after 3 months. conditions: Tooth Sensitivity studyType: IN... |
<|newrecord|> nctId: NCT06288763 id: SC220192 briefTitle: Nerve Transfer to Improve Function in High Level Tetraplegia overallStatus: RECRUITING date: 2024-02-05 date: 2028-03-01 date: 2028-12-31 date: 2024-03-01 date: 2024-04-02 name: Washington University School of Medicine class: OTHER name: University of Michigan n... |
Participants will: |
* undergo standard of care pre- and post-op testing and study exams |
* complete pre- and post-questionnaires |
* undergo standard of care nerve transfer surgeries |
* follow-up with surgeon at 6/12/18/24/36 and potentially at 48 months |
* attend therapy at local therapist for up to 2 years postop. conditions: Cervical Spinal Cord Injury conditions: Tetraplegia studyType: OBSERVATIONAL observationalModel: CASE_ONLY timePerspective: PROSPECTIVE count: 30 type: ESTIMATED measure: Elbow Dynamometry measure: Spinal Cord Independence Measure measure: Motor ... |
<|newrecord|> nctId: NCT06288750 id: sdllycyyqx001 briefTitle: Protective Effect of Indocyanine Green Fluorescence Imaging Technology on Parathyroid Glands During Total Thyroidectomy overallStatus: RECRUITING date: 2024-02-01 date: 2025-06-01 date: 2025-06-30 date: 2024-03-01 date: 2024-03-05 name: Shandong Linglong Yi... |
<|newrecord|> nctId: NCT06288737 id: 54335073 briefTitle: Assessing Patient Engagement in Keratoconus Clinical Research overallStatus: NOT_YET_RECRUITING date: 2025-03 date: 2026-03 date: 2027-03 date: 2024-03-01 date: 2024-03-01 name: Power Life Sciences Inc. class: INDUSTRY briefSummary: This study aims to investigat... |
In essence, this trial aims to deepen understanding of the factors influencing participation in keratoconus clinical trials. Elevating participation rates could expedite the development of innovative treatments for this challenging condition. conditions: Keratoconus studyType: OBSERVATIONAL observationalModel: CASE_CRO... |
<|newrecord|> nctId: NCT06288724 id: NatIntensive briefTitle: MOdifiable facTors to Improve VentilAtion ThErapy in ICU acronym: MOTIVATE-ICU overallStatus: NOT_YET_RECRUITING date: 2024-03 date: 2024-09 date: 2024-09 date: 2024-03-01 date: 2024-03-01 name: Nat Intensive Care Surveillance - MORU class: OTHER name: D'Or ... |
Methods: The MOTIVATE-ICU is a prospective multicentre observational study in invasively ventilated patients. It involves a registry-embedded component examining patient- and process-related factors and a cross-sectional survey on ICU organizational structures. Inclusion criteria encompass patients aged ≥ 15 years unde... |
Ethics and Dissemination: Given its observational nature, this study seeks a waiver for patient individual informed consent. Data anonymization ensures patient privacy. Following the principles of the Declaration of Helsinki, relevant ethical approvals will be acquired. Study findings will be disseminated through confe... |
<|newrecord|> nctId: NCT06288711 id: CHRBSS #STUDY00002538 id: R01DA057308 type: NIH link: https://reporter.nih.gov/quickSearch/R01DA057308 briefTitle: Novel Telemedicine-Delivered Prolonged Exposure Therapy for Treating PTSD in Individuals With OUD overallStatus: RECRUITING date: 2024-04-30 date: 2027-08-31 date: 2027... |
<|newrecord|> nctId: NCT06288698 id: 53955721 briefTitle: Understanding Patient Engagement Trends in TBI Clinical Research overallStatus: NOT_YET_RECRUITING date: 2025-03 date: 2026-03 date: 2027-03 date: 2024-03-01 date: 2024-03-01 name: Power Life Sciences Inc. class: INDUSTRY briefSummary: Clinical trials, specifica... |
The main goal is to thoroughly scrutinize trial completion rates and voluntary withdrawals among this particular group of patients. conditions: TBI studyType: OBSERVATIONAL observationalModel: CASE_CROSSOVER timePerspective: PROSPECTIVE count: 500 type: ESTIMATED measure: Number of TBI patients who decide to enroll in ... |
<|newrecord|> nctId: NCT06288685 id: 73/256 id: 73/256 type: OTHER domain: Police General Hospital briefTitle: Percutaneous Trigger Finger Release Concomitant Steroid Injection Versus Percutaneous Trigger Finger Release Alone overallStatus: COMPLETED date: 2023-10-11 date: 2024-01-23 date: 2024-01-30 date: 2024-03-01 d... |
Percutaneous A1 pulley release is a cost-effective and straightforward procedure with outcomes comparable to open A1 pulley release. Postoperative pain is a prevalent concern. Corticosteroid injection is a common nonoperative treatment for trigger finger, providing favorable outcomes but associated with a notable risk ... |
Objective: |
To conduct a comparative analysis of early postoperative outcomes between percutaneous A1 pulley release with steroid injection and percutaneous A1 pulley release alone. |
Study Design \& Methods: |
This study constitutes a randomized controlled trial involving patients with trigger finger who underwent percutaneous release surgery from October 2023 to January 2024. A total of 38 patients were enrolled, with 18 assigned to the percutaneous A1 pulley release with steroid injection group and 20 to the percutaneous A... |
Patients were enrolled and randomized into two groups, percutaneous A1 pulley release with steroid injection (Group A) and percutaneous A1 pulley release alone (Group B), by utilizing computer generate randomization and the results were put in opaque sealed envelopes. Informed consent was obtained from all participants... |
<|newrecord|> nctId: NCT06288672 id: 1002 briefTitle: IBS Skin Patch Test Food Allergy Study overallStatus: RECRUITING date: 2023-08-15 date: 2025-12 date: 2025-12 date: 2024-03-01 date: 2024-03-01 name: IBS-80, LLC class: INDUSTRY briefSummary: Participants with IBS are skin patch tested (no needles) to 80 different f... |
<|newrecord|> nctId: NCT06288659 id: KY2024-050 briefTitle: aSAH Treatment Based on Intraventricular ICP Monitoring: A Prospective, Multicenter, Randomized and Controlled Trial acronym: ASTIM-MT overallStatus: NOT_YET_RECRUITING date: 2024-05-01 date: 2026-06-30 date: 2026-12-30 date: 2024-03-01 date: 2024-04-23 name: ... |
<|newrecord|> nctId: NCT06288646 id: ROMEO 101712 briefTitle: Using Infrared Spectroscopy to Analyze Volatile Organic Compounds (VOCs) in the Breath of Patients With Lung Cancer overallStatus: RECRUITING date: 2023-04-24 date: 2024-04-24 date: 2024-12-15 date: 2024-03-01 date: 2024-03-01 name: Picomole Inc class: INDUS... |
Participants will be asked to provide one breath sample, and two if they get treated. They will also be asked to fill out a questionnaire about their background and medical history. conditions: Lung Cancer conditions: Non Small Cell Lung Cancer studyType: OBSERVATIONAL observationalModel: CASE_CONTROL timePerspective: ... |
<|newrecord|> nctId: NCT06288633 id: FNWMRC briefTitle: Cardioneuroablation for Bradyarrhythmia acronym: CARDIOBOOST overallStatus: RECRUITING date: 2024-03-04 date: 2026-02-01 date: 2027-02-01 date: 2024-03-01 date: 2024-03-05 name: Federal State Budgetary Institution, V. A. Almazov Federal North-West Medical Research... |
<|newrecord|> nctId: NCT06288620 id: MA-EBC-II-024 briefTitle: Microwave Ablation in the Treatment of Early-stage Unifocal Invasive Breast Cancer overallStatus: RECRUITING date: 2024-02-25 date: 2025-05-10 date: 2025-05-30 date: 2024-03-01 date: 2024-03-01 name: The First Affiliated Hospital with Nanjing Medical Univer... |
<|newrecord|> nctId: NCT06288607 id: 2023-SR-708 briefTitle: Safety and Efficacy of High Intensity Focused Ultrasound in Solar Lentigo: A Self-controlled Study overallStatus: ACTIVE_NOT_RECRUITING date: 2023-11-16 date: 2024-04-18 date: 2024-04-18 date: 2024-03-01 date: 2024-03-06 name: The First Affiliated Hospital wi... |
<|newrecord|> nctId: NCT06288594 id: DEU-PSI-HA-001 briefTitle: TraumaRelief App: A Pilot RCT Assessing Feasibility and Acceptability overallStatus: NOT_YET_RECRUITING date: 2024-06 date: 2024-09 date: 2024-12 date: 2024-03-01 date: 2024-03-06 name: Dokuz Eylul University class: OTHER briefSummary: The world experience... |
<|newrecord|> nctId: NCT06288581 id: UDDS-Pedo-02-2024 briefTitle: U Shaped Toothbrush in Removing Plaque in Children overallStatus: RECRUITING date: 2024-02-01 date: 2024-05-01 date: 2024-08-01 date: 2024-03-01 date: 2024-03-01 name: Damascus University class: OTHER briefSummary: The aim of this study is to evaluate t... |
Children accepted in the study will be randomly divided into two groups: |
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