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Syndrome clinical trials

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NCT ID: NCT05098678 Completed - Behcet Syndrome Clinical Trials

Zinc Supplementation and Behçet's Syndrome

Start date: August 22, 2020
Phase: N/A
Study type: Interventional

To study the effects of zinc gluconate supplementation on patients with Behçet's syndrome, 50 patients will be randomly allocated to two groups: placebo group or zinc group (one tablet of 30 mg/day elemental zinc) for 12 weeks. All participants will be asked not to alter their diet, medication, and physical activity during the study. At the first and the end of the intervention, genes and proteins expression, the serum level of inflammatory factors, quality of life, disease activity, anthropometric measures, physical activity and serum level of zinc will be assessed and compared between groups.

NCT ID: NCT05097222 Completed - Clinical trials for Mild Traumatic Brain Injury

Impact of Photobiomodulation on Objective, Physiological Measures of Brain Function in Individuals With Post-Concussion Syndrome

Start date: January 27, 2022
Phase: N/A
Study type: Interventional

Photobiomodulation therapy (PBMT) uses light to influence the mitochondria of cells. PBMT of the brain enhances the metabolic capacity of neurons and stimulates anti-inflammatory, anti-apoptotic, and antioxidant responses, as well as neurogenesis and synaptogenesis. Its therapeutic role in disorders such as dementia and Parkinson's disease, as well as to treat stroke, brain trauma, and depression has gained increasing interest. BioFlex is a form of PBMT consisting of light-emitting diodes (LEDs) and laser diodes. BioFlex utilizes red and near infrared light which penetrates tissues up to a certain tissue depth and studies have shown stimulates tissue growth and repair at the cellular level. PBMT has been proven useful for the treatment of soft tissue pain. Several studies have shown benefit in using PBMT in the treatment of certain neurological conditions, including chronic, mild traumatic brain injury (mTBI). The purpose of this exploratory investigation, therefore, is to examine efficacy of BioFlex laser therapy on measures of brain function in patients suffering from PCS after mild-moderate, closed-head, traumatic brain injury cases.

NCT ID: NCT05094778 Completed - Clinical trials for Carpal Tunnel Syndrome

A Single-portal Endoscopic Approach Through Subcutaneous Tunnel for Carpal Tunnel Release

Start date: January 5, 2012
Phase: N/A
Study type: Interventional

Traditional endoscopic release directly accesses the carpal tunnel and thus carries a higher risk of nerve irritability, even nerve injury. Based on our anatomical study, the investigators developed a new endoscopic technique through a single-portal palm approach that passes superficially to palmar aponeurosis, and cut the full transverse carpal ligament. The investigators will compared the technique with the standard dual-portal endoscopic technique.

NCT ID: NCT05092178 Completed - Metabolic Syndrome Clinical Trials

Calorie Restricted Diet and Exercise

Start date: January 6, 2019
Phase: N/A
Study type: Interventional

Calorie-restricted(CR) diet and exercise were effective to reduce Metabolic syndrome(MetS), however, its effect on knee functions for MetS patients with degenerate meniscus lesions(DMLs) was still poorly investigated.

NCT ID: NCT05088434 Completed - Clinical trials for Irritable Bowel Syndrome

Fecal Microbiota Transplantation and ACHIM for Manipulating Gut Microbiota in IBS Patients

Start date: January 1, 2017
Phase: N/A
Study type: Interventional

The double-blinded placebo-controlled study compares the effect of fecal microbiota transplantation vs. Anaerobically Cultivated Human Intestinal Microbiota (ACHIM) or placebo (own feces) on manipulating the gut microbiota in patients with diarrhea-predominant irritable bowel syndrome (IBS).

NCT ID: NCT05086042 Completed - Clinical trials for Carpal Tunnel Syndrome

Carpal Tunnel Syndrome in Patients With Psoriatic Arthritis; Ultrasonography and Magnetic Resonance Imaging Findings

Start date: March 15, 2019
Phase:
Study type: Observational

This study aimed to investigate relationship between CTS diagnosis with electrodiagnostic studies and median nerve's cross-sectional area measered by US and MRI in PsA patients.

NCT ID: NCT05086029 Completed - Clinical trials for Carpal Tunnel Syndrome

Carpal Tunnel Syndrome in Patients With Psoriatic Arthritis

Start date: March 20, 2019
Phase:
Study type: Observational

This study aimed to investigate median nerve hypervasculatitation in psoriatic arthritis (PsA) patients with CTS or without CTS by using SMI, then compare them with normal people.

NCT ID: NCT05085821 Completed - Clinical trials for Chronic Pain Syndrome

Cardio-visual Stimulation in Augmented Reality for Pain Reduction

HEART
Start date: April 20, 2021
Phase: N/A
Study type: Interventional

The objective of this study is to evaluate the feasibility and efficacy of an Augmented Reality (AR) biofeedback intervention to alleviate pain symptoms in individuals suffering from chronic pain of the hand and/or the forearm.

NCT ID: NCT05083130 Completed - COVID-19 Clinical Trials

Awake Prone Positioning in Moderate to Severe COVID-19

Start date: March 8, 2022
Phase: N/A
Study type: Interventional

The purpose of this study is comparing vital signs between standard care and prone position groups. Standard care will consist of routine clinical care, including any advice to lie in prone position as routinely recommended by participating sites. For those randomized to prone position, a special intervention team will visit patients' rooms aiming for patients to maintain the prone position for at least 8 hours a day.

NCT ID: NCT05078333 Completed - Clinical trials for Myofascial Pain Syndrome

Dry Needling and High Intensity Laser Therapy in Treatment of Myofascial Pain Syndrome

Start date: August 16, 2021
Phase: N/A
Study type: Interventional

108 myofascial pain syndrome (MPS) diagnosed patients will be randomly divided into 3 groups. To groups; exercise, exercise+high-intensity laser therapy (HILT) and exercise+dry needling will be applied. Visual anolog scale (VAS) scores and neck range of motion (ROM) of the patients before-after treatment will be recorded and will be evaluated statistically.