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Myalgia clinical trials

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NCT ID: NCT06402162 Active, not recruiting - Exercise Clinical Trials

The Effect of Core Stability Exercises on Pain, Muscle Strength, and Muscle Architecture in Tennis Players With Rotator Cuff Lesions

Start date: May 1, 2023
Phase: N/A
Study type: Interventional

This study aims to shed light on the supraspinatus and infraspinatus muscles, which play a significant role in rotator sheath tendinopathy and tears. It includes isometric measurements of muscle thickness, fiber length, and pennation angles, as well as muscle strength, using ultrasound to evaluate the muscle architecture of the supraspinatus and infraspinatus muscles in tennis players.

NCT ID: NCT06076356 Active, not recruiting - Clinical trials for Delayed Onset Muscle Soreness

Effects of Foam Roller Versus KT Tape on Delayed Onset Muscle Soreness

Start date: August 15, 2023
Phase: N/A
Study type: Interventional

Objective of this study is to compare the effects of foam roller with KT tape on DOMS. The university going students will be divided in two groups, with one group receiving Kinesio Tape as intervention and other Foam Rolling as intervention. Pain and range of motion will be assessed before and after the intervention and the effects of both interventions will be compared.

NCT ID: NCT05664711 Active, not recruiting - Clinical trials for Chronic Fatigue Syndrome

Effect of Stellate Ganglion Block on ME/CFS

SGB_ME
Start date: March 15, 2023
Phase: Phase 1
Study type: Interventional

The goal of this clinical trial is to study the effects of stellate ganglion block (SGB) in participants with myalgic encephalomyelitis/chronic fatigue syndrome (ME/CFS). The main questions it aims to answer are: Does SGB treatment improve symptoms of ME/CFS (e.g. brain fog, fatigue)? Do changes in symptoms go along with changes in blood or saliva? Participants will receive a total of six blocks over three weeks (one block on each side, one day apart, per week). Prior to treatment and at two points following treatment, participants will complete surveys, take a cognitive (puzzle type) test, and provide blood and saliva for analysis. Participants will measure their heart rate daily using a free smart phone app.

NCT ID: NCT04927741 Active, not recruiting - IUD Clinical Trials

Essential Oils Following IUD Insertion

Start date: May 27, 2021
Phase: N/A
Study type: Interventional

This study will measure the effects of topical application of sweet marjoram essential oil + grapeseed oil with massage on uterine cramping/pain post-IUD insertion/placement. The intention is to conduct a pilot study that could give a first look at the data to determine whether this line of research is worth pursuing with more time, effort, and resources. The results of this pilot study will provide adequate data (e.g., variance estimates) needed for obtaining reasonably reliable sample size estimates if larger studies are warranted in the future.

NCT ID: NCT04622293 Active, not recruiting - Clinical trials for Chronic Fatigue Syndrome

A Trial of Solriamfetol in the Treatment of Myalgic Encephalomyelitis/Chronic Fatigue Syndrome

Start date: April 27, 2021
Phase: Phase 4
Study type: Interventional

This study is an 8-week single center, randomized, double-blind, placebo-controlled, flexible titration trial evaluating the efficacy of solriamfetol in the treatment of fatigue symptoms in adult patients with chronic fatigue syndrome. Subjects will be randomized to a solriamfetol group or placebo group. The investigators will utilize an intent to treat model and impute data. The overall goal of this study is to determine the efficacy and effectiveness of solriamfetol for treating chronic fatigue syndrome.

NCT ID: NCT02997410 Active, not recruiting - Clinical trials for Temporomandibular Joint Disorders

Ozone Therapy for Masticatory Muscle Pain (OTMMP)

OTMMP
Start date: December 2014
Phase: N/A
Study type: Interventional

This study investigates the efficacy of bio-oxidative ozone application in the treatment of TMD of muscular origin.

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: NCT02843269 Active, not recruiting - Neck Pain Clinical Trials

Multiple-component Workplace FRamed Intervention to Decrease Occupational Muscle Pain - FRIDOM

FRIDOM
Start date: September 2014
Phase: N/A
Study type: Interventional

Several RCT studies have aimed to reduce either musculoskeletal disorders, sickness presenteeism, sickness absenteeism or a combination of these among females with high physical work demands. These studies have provided evidence that workplace health promotion (WHP) interventions are effective, but long-term effects are still uncertain. These studies either lack to succeed in maintaining intervention effects or lack to document if effects are maintained past a one-year period. FRIDOM (FRamed Intervention to Decrease Occupational Muscle pain) is a WHP program among health care workers. A job group characterized by having high physical work demands, musculoskeletal disorders, high sickness presenteeism - and absenteeism. FRIDOM aimed to reduce neck and shoulder pain and secondary to reduce sickness presenteeism and sickness absenteeism. An other secondary aim was to decrease lifestyle-diseases such as other musculoskeletal disorders as well as metabolic-, and cardiovascular disorders - and to maintain participation to regular physical exercise training, after a one year intervention period. The entire concept was tailored to a population of female health care workers. This was done through a multi-component intervention including 1) intelligent physical exercise training (IPET), dietary advice and weight loss (DAW) and cognitive behavioural training (CBT).

NCT ID: NCT01032993 Active, not recruiting - Pain Clinical Trials

Clinical Trial of CoQ10 for Mild-to-Moderate Statin-Associated Muscle Symptoms

Start date: December 2009
Phase: Phase 2/Phase 3
Study type: Interventional

This study will evaluate whether a dietary supplement, coenzyme Q10 (CoQ10), will improve muscle symptoms, such as muscle aches, pains, cramps, and/or weakness, which are experienced by some individuals who use statin medications.