Clinical Trials Logo

Chronic Fatigue Syndrome clinical trials

View clinical trials related to Chronic Fatigue Syndrome.

Filter by:

NCT ID: NCT03254823 Enrolling by invitation - Clinical trials for Chronic Fatigue Syndrome

Autoimmunity in Myalgic Encephalomyelitis/Chronic Fatigue Syndrome (ME/CFS)

Start date: March 28, 2018
Phase:
Study type: Observational

This study investigates whether there is an immune response directed against gut microbes or food and parts of the body in severe Myalgic Encephalomyelitis/Chronic Fatigue Syndrome (ME/CFS) patients.

NCT ID: NCT03186027 Completed - Clinical trials for Chronic Fatigue Syndrome

Coenzyme Q10 Plus NADH Supplementation in Chronic Fatigue Syndrome/Myalgic Encephalomyelitis

CONNeCT
Start date: June 28, 2017
Phase: N/A
Study type: Interventional

The main aim of the study is to examine the effect of oral CoQ10 plus NADH (Reconnect®) supplementation twice daily for 8-weeks on the changes in fatigue perception, sleep disturbances, autonomic dysfunction and HRQoL assessed by patient-reported outcome measures in CFS/ME.

NCT ID: NCT03075254 Active, not recruiting - Fibromyalgia Clinical Trials

Central Mechanisms of Chronic Pain and Fatigue Subtitle: Functional Imaging of Brain and Spinal Cord

Start date: March 15, 2017
Phase:
Study type: Observational

Chronic pain and fatigue are characterized by peripheral and central mechanisms including low pain thresholds, temporal summation, peripheral and central sensitization. This application will focus on central factors of chronic pain and fatigue. Functional brain imaging will be used to characterized brain and spinal cord abnormalities that contribute to the mechanisms of these disorders.

NCT ID: NCT03029377 Completed - Clinical trials for Chronic Fatigue Syndrome

Noradrenergic and Stress-Related Etiologies of Chronic Fatigue Syndrome

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

The objective of this study is to measure sympathetic nervous system function and stress responses in patients with clinically documented and self-reported chronic fatigue that is worsened by stress, compared to healthy controls. Baseline norepinephrine (NE) levels and stress-induced NE levels in patients who fulfill criteria for Chronic Fatigue Syndrome (CFS) and who self-identify with stress induced worsening fatigue, will be compared to data from normal individuals pre and post-stress.

NCT ID: NCT02970240 Completed - Clinical trials for Chronic Fatigue Syndrome

Cardiopulmonary Testing in ME/CFS to Improve Diagnostic Accuracy

Start date: June 2014
Phase:
Study type: Observational

Circumstantial evidence suggests that patients diagnosed with myalgic encephalopathy/chronic fatigue syndrome (ME/CFS) perform worse on day 2 in a 2-day consecutive cardiopulmonary exercise test (CPET). The aim of this study is to examine if CPET can distinguish between ME/CFS patients and healthy controls.

NCT ID: NCT02964533 Recruiting - Clinical trials for Chronic Fatigue Syndrome

Thunder-Fire Moxibustion Therapy for Chronic Fatigue Syndrome on Shenque Acupoint: a Randomized Controlled Trial

Start date: November 2016
Phase: N/A
Study type: Interventional

Chronic fatigue syndrome is a group of syndrome and is prevalent in adult. Thunder-fire moxibustion is a commentary therapy belonged to acupuncture therapy. To evaluate the effect and safety of thunder-fire moxibustion therapy for chronic fatigue syndrome, we apply a randomized controlled trial by recruiting chronic fatigue syndrome patient as subject, applying thunder-fire moxibustion on shenque acupoint contrasted to common moxa-stick moxibustion, taking fatigue rating scale score, the content of CD3+、CD4+、CD8+、CD4+/CD8+ as evaluation indexes. The treatment time is 20-30 minutes per session, 3-4 times a week, there are totally 15 sessions.

NCT ID: NCT02948556 Recruiting - Clinical trials for Chronic Fatigue Syndrome

ME/CFS: Activity Patterns and Autonomic Dysfunction

Start date: June 2016
Phase: N/A
Study type: Observational

The purpose of this study is to identify daily activity patterns, negative life events and autonomic abnormalities that may be related to non-improvement in myalgic encephalomyelitis/chronic fatigue syndrome (ME/CFS). For both naturalistic studies and behavioral intervention trials, roughly 50% of patients report worsening or unchanged illness. The proposed four year study would be the first to look at the relation between illness non-improvement, patient activities at home and autonomic function. Our long-range goal is to identify physiological signals and activity patterns that predict non-improvement and relapse and develop a self-management program that prescribes improvement-linked behaviors and discourages non-improvement activities.

NCT ID: NCT02924831 Not yet recruiting - Clinical trials for Chronic Fatigue Syndrome

High-tech Acupuncture for Treatment of Chronic Fatigue Syndrome

Start date: November 2016
Phase: Phase 2
Study type: Interventional

1. To study the relationship between Chronic Fatigue Syndrome (CFS) and heart rate (HR) and its variability (HRV). 2. To compare the curative effects and the HR/HRV indices between applicationa of different acupoints as well as different treatments (acupuncture and moxibustion).

NCT ID: NCT02854683 Active, not recruiting - Clinical trials for Chronic Fatigue Syndrome

Reducing Orthostatic Intolerance With Oral Rehydration in Myalgic Encephalomyelitis/Chronic Fatigue Syndrome Patients

Start date: February 2016
Phase: Phase 1
Study type: Interventional

We and others have shown that many younger patients with Myalgic Encephalomyelitis/Chronic Fatigue Syndrome (ME/CFS) have orthostatic intolerance (OI), i.e., they can't tolerate prolonged standing. OI in ME/CFS is often accompanied by either postural tachycardia syndrome (POTS) in which standing results in an excessive heart rate, and neurally mediated hypotension (NMH) in which standing causes a fall in blood pressure and fainting. Intravenous fluids can alleviate these symptoms, but is difficult to administer; oral fluids fail to provide the same benefit. We would therefore like to test the effectiveness of an oral rehydration solution (ORS, W.H.O. formula) making use of co-transport of glucose and sodium, to reverse these symptoms in ME/CFS subjects with POTS or NMS, and will compare these results with healthy control subjects.

NCT ID: NCT02847845 Recruiting - Clinical trials for Chronic Fatigue Syndrome

A Clinical Study About Improvement of Chronic Fatigue After Taking Red Ginseng

Start date: June 2016
Phase: N/A
Study type: Interventional

The purpose of this study is to verify the efficacy of taking red ginseng for chronic fatigue patient.