Clinical Trials Logo

Syndrome clinical trials

View clinical trials related to Syndrome.

Filter by:

NCT ID: NCT04044066 Recruiting - Clinical trials for Acute Coronary Syndrome

Biomarker-based Prognostic Assessment

Start date: November 9, 2017
Phase:
Study type: Observational [Patient Registry]

Coronary artery disease (including stable angina and acute coronary disease) remains the leading mortality and morbidity worldwide. Improvement in biomarker, imaging research have led to new predictors for the prognosis, which may have great clinical value in the current era of personalized medicine. However, there is no available biomarker-based prediction rule for risk assessment of adverse events in patients with stable angina and acute coronary disease. Therefore, we aim to develop and validate a new biomarker-based risk model to improve the prognostication of adverse events (e.g. ischemic and bleeding events ) in the patient population.

NCT ID: NCT04040842 Recruiting - Clinical trials for Low Anterior Resection Syndrome

International Low Anterior Resection Score Evaluation

PrePostLARS
Start date: September 1, 2019
Phase:
Study type: Observational

- Aim: The aim of this study is to perform a prospective, international 4 months cohort study evaluating bowel function before curative rectal cancer surgery and one year after the surgery using the LARS score. - Primary outcome measure: LARS score before surgery and 1 year after the surgery. - Primary comparison: Between average LARS score before and after curative surgery and also comparing these with publish LARS score on normal population.

NCT ID: NCT04032639 Recruiting - Clinical trials for Prader-Willi Syndrome

Stress and Brain Response Using MEG in PWS

Start date: May 30, 2019
Phase:
Study type: Observational

Individuals with Prader-Willi Syndrome (PWS) have increased hunger and food seeking behaviour, as well as learning (cognitive) challenges. In addition, some patients with PW been shown to have low cortisol production, particularly in stressful situations. However, research examining how hormonal, cognitive, and psychological factors are interrelated PWS is limited. To address this gap in knowledge, the goal of this project is to understand how changes in brain regions involved in controlling food intake and cognitive processes are related to changes in hormones regulating appetite, the stress hormone cortisol, and performance on neuropsychological tests.

NCT ID: NCT04029805 Recruiting - Insulin Resistance Clinical Trials

Evaluation of a Combination of a Plant Extract and a Probiotic on Glucidic Metabolism in Women With PCOS and High Insulin Levels

Start date: May 29, 2019
Phase: Phase 1/Phase 2
Study type: Interventional

The aim of the present study is to evaluate the effect of the combination of a plant extract (BSL_EP044) and Lactobacillus BSL_PS6 on parameters of the glucidic metabolism, anthropometric parameters, hormonal levels and the menstrual cycle in women with polycystic ovary syndrome and high insulin levels.

NCT ID: NCT04029272 Recruiting - Clinical trials for Polycystic Ovary Syndrome

Metformin vs Metformin Combined With GLP-1RA (Glucagon-like Peptide 1 Receptor Agonist) on Overweight/Obese PCOS Patients

Start date: July 20, 2019
Phase: Phase 4
Study type: Interventional

The purpose of this study was to determine whether metformin combined with exenatide once weekly (EQW) is more effective than metformin alone in the treatment of overweight/obese women with polycystic ovary syndrome (PCOS). Background therapies were Diane-35 or/and progesterone capsule. 80 participants were randomized to use either metformin or metformin+EQW for 12 weeks. Greater changes in body weight were anticipated in patients treated with EQW+metformin than metformin alone in those treated with metformin.

NCT ID: NCT04028193 Recruiting - Dumping Syndrome Clinical Trials

Fat Supplementation on Dumping Syndrome Associated Symptoms

Fat on DS
Start date: September 12, 2017
Phase: N/A
Study type: Interventional

The purpose of the study is the investigation of the effect of fat supplement on gastric emptying rate and the appearance of symptoms of Dumping Syndrome in patients who have undergone gastrointestinal- duodenal surgery. Patients who have undergone bariatric surgery have been examined for the presence of the Dumping syndrome, with glucose measurements, the Sigstad's questionnaire and questionnaire of Arts. Patients diagnosed positive, reiterated the examination process in a second meeting consuming an extra fat supplement. The data obtained on the different appointments were compared between the two groups in a cross over design.

NCT ID: NCT04027998 Recruiting - Clinical trials for Carpal Tunnel Syndrome

Median Nerve Strain and Applied Pressure Measurement in the Carpal Tunnel Syndrome Patients

Start date: April 3, 2015
Phase:
Study type: Observational

The aim of this study is to investigate diagnostic accuracy of median nerve strain and applied pressure measurement . Idiopathic carpal tunnel syndrome patients and healthy controls will be evaluated by ultrasound. Median nerve strain, pressure applied to the skin will be measured at the proximal part of the carpal tunnel. The parameters will be compared between patients and controls, and before and after the open carpal tunnel release in the patients.

NCT ID: NCT04025203 Recruiting - Clinical trials for Carpal Tunnel Syndrome

Pain Reduction and Changes in Upper Limb Function Produced by Different Treatments in Carpal Tunnel Syndrome

Start date: August 1, 2019
Phase: Phase 4
Study type: Interventional

In the present investigation the pain reduction effects of a physiotherapy technique will be compared to those produced by two different pharmaceutical treatments and also by the absence of treatment, in subjects who suffer the signs and symptoms of carpal tunnel syndrome.

NCT ID: NCT04023565 Recruiting - Metabolic Syndrome Clinical Trials

Moxonidine + Perindopril in Hypertensive Patients With Metabolic Syndrome

COMPOSER
Start date: March 11, 2019
Phase: Phase 4
Study type: Interventional

The aim of study is to assess the angioprotective effects of antihypertensive combination therapy with perindopril 10 mg and moxonidine 0.4-0.6 mg in patients with arterial hypertension, metabolic syndrome, and obesity, who had Pulse Wave Velocity (PWV) > 10 m/s on the previously administered two-component combination antihypertensive therapy. Open-label non-comparative prospective study for 24 week for each patient.

NCT ID: NCT04023448 Recruiting - Rectal Cancer Clinical Trials

The Effect of Different Reconstruction Methods on Anterior Resection Syndrome

TEDRMARS
Start date: September 1, 2019
Phase: N/A
Study type: Interventional

The incidence of prerectal resection syndrome (LARS) after middle and low rectal cancer surgery is as high as 70%, which seriously affects the quality of life of patients. Studies have shown that colon pouch can reduce and alleviate LARS symptoms. However, most previous studies focused on open surgery, and the evaluation index lacked objectivity. Therefore, in the context of minimally invasive rectal cancer surgery, it is necessary to re-evaluate the value of improved surgical methods for the prevention of LARS, so as to improve the quality of life of patients.