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NCT ID: NCT04776343 Not yet recruiting - Clinical trials for Diabetic Macular Edema

Study Comparing Two Populations of Patients Treated With Anti VEGF for Diabetic Macular Edema, One Being Followed at the Hospital and the Other One Being Followed at Home Using a Software Allowing Self-assessment of Visual Acuity

Start date: April 2021
Phase: N/A
Study type: Interventional

Verify the reliability of VA measured every week at home, by the patient using a TC, compared to the reliability of VA also measured by the patient using a TC but every 2 month at the hospital, during standard DME follow-up visits

NCT ID: NCT04777448 Not yet recruiting - Clinical trials for Chronic Thromboembolic Pulmonary Hypertension

Optimized Management After Balloon Pulmonary Angioplasty in Chronic Thromboembolic Pulmonary Hypertension

POpPART
Start date: April 2021
Phase: N/A
Study type: Interventional

Balloon pulmonary angioplasty (BPA) is a new method of treatment for inoperable chronic thromboembolic pulmonary hypertension (CTEPH) or persistent CTEPH after surgery. BPA improves or even normalises hemodynamic parameters measured during a right heart catheterization. Nevertheless, the vast majority of patients retain dyspnea and impaired exercise capacity despite considerable hemodynamic improvements. Pulmonary rehabilitation (RHB) can improve symptoms, quality of life and exercise capacity in patients with CTEPH. Unfortunately, access to RHB remains a concern in many countries. Tele-rehabilitation (tRHB) has been shown feasible and effective some cardiac or pulmonary diseases. This randomized controlled study aims at comparing the effects of tRHB with the effects of simple advices regarding exercising in CTEPH patients with normalized or near-normalized pulmonary hemodynamics after BPA treatment.

NCT ID: NCT04779359 Not yet recruiting - COVID-19 Disease Clinical Trials

Role of Lymphocyte Subsets and Laboratory Measurements in COVID-19 Disease

Start date: April 2021
Phase:
Study type: Observational [Patient Registry]

To investigate the predictive role of lymphocyte subsets and other laboratory measurements in adult patients with COVID-19.This was a single center, retrospective study that involved adult patients with confirmed diagnosis of COVID-19. Electronic medical records were reviewed. Data including age, sex, symptom from onset to hospital admission and laboratory findings at admission of hospitalized patients with confirmed COVID-19 were extracted and analyzed retrospectively.This study indicates that the levels of lymphocyte subsets (CD4+, and CD8+) are associated with disease progression and severity, along with prognosis in patients with COVID-19.

NCT ID: NCT04782440 Not yet recruiting - Clinical trials for Duchenne Muscular Dystrophy

The Effect of Telerehabilitation of Patients With Duchenne Muscular Dystrophy

Start date: April 2021
Phase: N/A
Study type: Interventional

The aim of this study is to investigate the effect of a telerehabilitation approach to patients with Duchenne Muscular Dystrophy and evaluate patients' motor function, parents' anxiety and depression levels before and after the intervention

NCT ID: NCT04782960 Not yet recruiting - Anesthesia, Local Clinical Trials

Subconjunctival Bupivacaine in Strabismus Surgery

Start date: April 2021
Phase: N/A
Study type: Interventional

This study aimed to assess the effectiveness of the Subconjunctival bupivacaine on postoperative pain in Strabismus surgery under general anaesthesia.

NCT ID: NCT04784169 Not yet recruiting - CSF Leakage Clinical Trials

Free Middle Turbinate Flap for Repair of Low Flow Cerebrospinal Fluid Leak

Start date: April 2021
Phase: N/A
Study type: Interventional

Limited literature has been reported the use of free middle turbinate flap during an endoscopic approach to treat cerebrospinal fluid (CSF) leak, and the results were inconclusive. The overall purpose of this study was to assess the efficacy and safety of free middle turbinate flap in reparing CSF leak during an endoscopic approach.

NCT ID: NCT04786418 Not yet recruiting - Obesity Clinical Trials

Low-Calorie Diet in People With Prediabetes/Metabolic Syndrome

CALIBRATE
Start date: April 2021
Phase: N/A
Study type: Interventional

Significant weight reduction, achieved by low-calorie diet (LCD), will mobilise ectopic fat (visceral and particularly liver fat), improving insulin sensitivity and other metabolic syndrome components, with secondary beneficial effects on cardiac structure and function. This CALIBRATE study (metabolic, multi-organ and effects of low-calorie diet in younger obese patients with pre-diabetes) will compare the effects of a safe and effective 12-month weight management intervention, initially using a low-calorie, liquid replacement diet for 12 weeks, anticipating at least 10% reduction in body weight. The investigators will examine how much the weight loss improves the metabolic abnormalities that precede type 2 diabetes (T2D), and in reversing the pre-clinical/subtle clinical abnormalities of the liver and heart that precede liver and cardiovascular disease (CVD). This study will compare the effects of a safe and effective 12-month weight management intervention, initially using a low-calorie, liquid replacement diet for 12 weeks, followed by a weight maintenance phase. The investigators will examine how much the weight loss improves the metabolic and neuropathic abnormalities that precede and accompany type 2 diabetes (T2D), and in reversing the pre-clinical/subtle clinical abnormalities of the liver and heart that precede liver and cardiovascular disease. In an additional optional sub-study, the investigators will additionally assess how the weight loss impacts upon appetite regulation within the brain with functional MRI (fMRI).

NCT ID: NCT04790006 Not yet recruiting - Type 2 Diabetes Clinical Trials

A Study of TG103 in Subjects With Type 2 Diabetes

Start date: April 2021
Phase: Phase 1
Study type: Interventional

The main purpose of this study is to assess the safety and tolerability of multiple ascending doses of TG103 in subjects with type 2 diabetes.

NCT ID: NCT04793256 Not yet recruiting - Cost Effectiveness Clinical Trials

Clinical and Cost-effectiveness of Fluoride Varnish Versus Resin Based Sealant (Part 2)

Start date: April 2021
Phase: N/A
Study type: Interventional

The aim of the present study is determine the cost-effectiveness, clinical- effectiveness, acceptability and adverse effect of resin sealants versus the fluoride varnish for the prevention of dental caries on newly erupted permanent molars.

NCT ID: NCT04795193 Not yet recruiting - Clinical trials for Coronary Artery Bypass, Off-Pump

Efficacy and Safety of Minimal Invasive Coronary Surgery in Patients With Complex Coronary Artery Lesions

Start date: April 2021
Phase: N/A
Study type: Interventional

The aim of this study is to investigate and compare the mid-term safety and efficacy end-points [medical outcomes study-short form 36-item (SF-36) physical component summary (PCS) at 30 days after surgery, etc.] in patients with complex coronary artery lesions [an indication of off-pump coronary artery bypass surgery (OPCAGB)] who received minimal invasive coronary surgery (MICS)-CABG and those who received thoracotomy OPCABG. The investigators hypothesize that patients in MICS-CABG group have superior clinical demonstrations regarding the primary endpoint than those in OPCAGB group without increased adverse outcomes. A total of 200 eligible patients are planned to be randomized to MICS-CABG or OPCABG group with an allocation ratio of 1:1. The primary endpoint is SF-36 PCS at 30 days after surgery. The analysis on primary endpoints will be conducted according to the basic principle of intention-to-treat (ITT).