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NCT ID: NCT05104697 Completed - Clinical trials for Obsessive-Compulsive Disorder

TMS for Improving Response Inhibition in Adolescents With OCD

Start date: April 1, 2022
Phase: N/A
Study type: Interventional

The study will examine whether inhibition of the pre-supplementary motor area (pSMA) using transcranial magnetic stimulation (TMS) normalizes activity in pSMA-connected circuits, improves response inhibition, and reduces compulsions in adolescents with OCD.

NCT ID: NCT05128929 Completed - Clinical trials for Pulmonary Hypertension

Investigation of H01 in Adults With Pulmonary Hypertension Including Interstitial Lung Disease (The SATURN Study).

SATURN
Start date: April 1, 2022
Phase: Phase 2
Study type: Interventional

This study is a prospective, randomized, double-blind, study of H01 (Hymecromone) in adults with pulmonary hypertension (PH). The primary objective of this study is to evaluate the safety and tolerability of oral H01 and the potential benefit of oral H01 on clinical measures of PH disease severity over 24 weeks. Study Hypothesis: Oral H01, at doses of 1600 mg per day, will be a safe and well-tolerated agent in adults with pulmonary hypertension over 24 weeks

NCT ID: NCT05140642 Completed - Clinical trials for Heart Failure, Systolic

Safety and Efficacy Study of AI LVEF

EchoNet-RCT
Start date: April 1, 2022
Phase: N/A
Study type: Interventional

To determine whether an integrated AI decision support can save time and improve accuracy of assessment of echocardiograms, the investigators are conducting a blinded, randomized controlled study of AI guided measurements of left ventricular ejection fraction compared to sonographer measurements in preliminary readings of echocardiograms.

NCT ID: NCT05169164 Completed - Clinical trials for Postoperative Complications

Latin American Surgical Outcomes Study

LASOS
Start date: April 1, 2022
Phase:
Study type: Observational [Patient Registry]

Methods: International, seven-day observational cohort study of complications following elective or emergency surgery. Objectives: To provide detailed data describing post-operative complications and associated mortality. Number of participants: Our aim is to recruit as many patients from as many hospitals as possible in Latin American nations. Eligible countries for participation: Countries and dependencies in Latin America that are situated in the area stretching from the northern border of Mexico to the southern tip of South America, including the Caribbean. Inclusion criteria: all adult patients aged 18 years or older undergoing elective or emergency surgery during the seven-day study period with a planned overnight stay. Exclusion criteria: patients who are undergoing planned day-case surgery or radiological procedures. Statistical methodology and analysis: Single and multi-level logistic regression models will be constructed to identify factors independently associated with these outcomes and to adjust for differences in confounding factors. A single final analysis is planned at the end of the study. A pre-defined analysis will focus on outcomes of patients who have undergone caesarean section. Study duration: Each nation will select a 7-day period between 1st April and 31th October 2022.

NCT ID: NCT05180903 Completed - Clinical trials for Dental Restoration Failure

Clinical Performance of Polyethylene Fiber Reinforced Resin Composite Restorations (Wall Papering Technique) Versus Bulk Fill Resin Composite Restorations in Endodontically Treated Teeth Will be Evaluated Using Modified USPHS Criteria.

Start date: April 1, 2022
Phase: N/A
Study type: Interventional

The aim of this study will be to evaluate the clinical performance of polyethylene fiber reinforced resin composite restorations versus bulk fill resin composite restorations in endodontically treated teeth.

NCT ID: NCT05187741 Completed - HIV I Infection Clinical Trials

Effect of a Mobile Health Intervention on Treatment Adherence

Start date: April 1, 2022
Phase: N/A
Study type: Interventional

This is a randomized clinical trial across the whole of the patients who attend the HIV Unit of the Hospital Civil Viejo, a sample calculated in 43 patients for each group (intervention and control). Patients who have HIV infection and are starting antiretroviral treatment (ART), who are between 18 and 50 years old and have a mobile device, will be included in the study. The messages will consist of medical appointment reminders and adherence and motivational messages for a period of six months.

NCT ID: NCT05188820 Completed - Low Back Pain Clinical Trials

Comparison of IntraArticular Platelet-Rich-Plasma to Corticosteroid Injections for Patients With Zygapophyseal Joint (Z-Joint) Low Back Pain Confirmed by Dual Intra-Articular Local Anesthetic Injections

Start date: April 1, 2022
Phase: N/A
Study type: Interventional

Comparison of IntraArticular Platelet-Rich-Plasma to Corticosteroid Injections for Patients with Zygapophyseal Joint (Z-Joint) Low Back Pain Confirmed by Dual Intra-Articular Local Anesthetic Injections: A Triple Blinded Randomized Controlled Trial.

NCT ID: NCT05195073 Completed - Hydrosalpinx Clinical Trials

Three Dimensional Versus Two Dimensional Laparoscopic Salpingectomy in Patients With Hydrosalpinx Undergoing IVF-ET

Start date: April 1, 2022
Phase: N/A
Study type: Interventional

A three-dimensional laparoscopic vision system (3-D LVS) has gained acceptance and is being utilized in daily practice despite debates about its success.

NCT ID: NCT05204992 Completed - Clinical trials for Carpal Tunnel Syndrome

Effectiveness of Ultrasound Guided Hydro-dissection of Median Nerve in Carpal Tunnel Syndrome

Start date: April 1, 2022
Phase: N/A
Study type: Interventional

60 patients with carpal tunnel syndrome will undergo ultrasound guided hydrodissection of the median nerve with follow up using Boston Carpal Tunnel Syndrome Questionnaire (BCTQ) at 3, 6 and 12 months

NCT ID: NCT05219227 Completed - Obesity, Abdominal Clinical Trials

Effect of Laser Acupuncture Augmented by Abdominal Exercises on Abdominal Fat

Start date: April 1, 2022
Phase: N/A
Study type: Interventional

the aim of study is to investigate the effect of laser acupuncture and abdominal exercises on abdominal fat in breast feeding women