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Myalgia clinical trials

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NCT ID: NCT02892994 Completed - Clinical trials for Temporomandibular Joint Dysfunction Syndrome

Immediate Effect of Ultrasound Therapy on Bilateral Masseter Myalgia

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

This study will compare ultrasound 0.4 W/cm^2 and 100% duty cycle versus no ultrasound (placebo) for bilateral masseter myalgia in up to 38 adult women. The dose will be applied for 5 minutes on each side. Both the dose and the starting side will be randomized. Both the subject and ultrasound operator will be blind to the dose. The outcome measures will be pressure pain threshold on both masseter muscles and both temporalis muscles, self reported pain scale (0, no pain to 10, worst pain ever), thermographic temperature of the muscles, and intraoral temperature. These outcome measures will be taken before and after each dose, so three times per subject.

NCT ID: NCT02806609 Completed - Pain Clinical Trials

Effect of Muscle Pain in Late Cold Water Immersion, Muscular Recruitment, Postural Control Dynamic and Sleep Quality

Start date: June 1, 2016
Phase: N/A
Study type: Interventional

Objective: To evaluate the effect of cold water immersion in elayed onset muscle soreness, muscle recruitment, dynamic postural control and quality of sleep in young soccer players. Methods: The sample will consist of 28 soccer players between 18 and 21 years of the same football club and with the same routine practices and games. At first athletes will respond to the IC and will be submitted to the test of a repetition maximum. After three days the athletes will analysis of muscle recruitment by electromyography and dynamic posture control through the force platform both during the time of shooting, moreover, will respond to scale the quality of sleep the previous night and one on pain, then they are instructed to perform a fatigue protocol for the quadriceps and then will be randomized to one of four intervention groups: cold water immersion, submersion in water at room temperature, or active recovery control. The same APPRAISAL be remade into three new moments, 24, 48 and 72 hours after the fatigue test. Hypothesis: The variables will be considered: Pain intensity in the quadriceps muscle, quality of sleep the night after intervention protocol, electromyographic analysis of the rectus femoris, vastus medialis oblique and vastus lateralis at the time of shooting, as well as postural control when the shot off. It is intended to establish the best way of recovery of late quadriceps muscle pain and contribute to the clinical practice of active recovery or rest in young soccer players.

NCT ID: NCT02746250 Completed - Clinical trials for Tension-type Headache

Muscle Soreness and Stiffness in Patients With Chronic or Frequent Episodic Tension Type Headache.

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

The aim is to investigate muscle soreness and stiffness in patients with Chronic or Frequent Episodic Tension Type Headache before and after treatment with amitriptyline - and to compare the results with healthy individuals.

NCT ID: NCT02695381 Completed - Clinical trials for Acute Delayed Onset Muscle Soreness (DOMS)

Etodolac-lidocaine Patch in Subjects Experiencing Acute Delayed Onset Muscle Soreness

Start date: March 2016
Phase: Phase 3
Study type: Interventional

This study evaluate the efficacy and safety of Etodolac-lidocaine topical patch applied one time daily when compared with placebo in the treatment of acute Delayed Onset Muscle Soreness (DOMS) of the upper limbs.

NCT ID: NCT02693678 Completed - Clinical trials for Musculoskeletal Pain

Real and Sham Diathermy vs Hand Massage in Lower Limbs Delayed Onset Muscle Soreness (DOMS)Effect on Knee Proprioception

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

Delayed onset muscle soreness (DOMS) can have an impact on the proprioception of knee joint . The study aim is to assess the effect of manual massage, diathermy and sham diathermy the proprioception of the knee joint in patients affected by DOMS.

NCT ID: NCT02602353 Completed - Clinical trials for Delayed Onset Muscle Soreness

Pilot Study Comparing the Efficacy and Safety of a New Pain Patch and Placebo in Delayed Onset Muscle Soreness (DOMS)

Start date: October 2015
Phase: Phase 2
Study type: Interventional

The purpose of this study is to evaluate the analgesic efficacy and safety of a new pain patch compared to placebo and no treatment in subjects experiencing Delayed Onset Muscle Soreness (DOMS).

NCT ID: NCT02597634 Completed - Clinical trials for Delayed Onset Muscle Soreness, DOMS

Study of SST-0225 Topical Ibuprofen Cream in the Treatment of Delayed Onset Muscle Soreness (DOMS)

DOMS
Start date: November 2015
Phase: Phase 3
Study type: Interventional

This is a Phase 3, prospective, randomized, dual-center, double-blind, placebo-controlled, parallel-group study designed to determine the efficacy and safety of SST-0225 (5.4 grams, applied up to 6 times in 24 hours, over a 48-hour dosing period) for the treatment of pain associated with DOMS.

NCT ID: NCT02548208 Completed - Clinical trials for Musculoskeletal Pain

Single Focused Shock Wave in the Release od Delayed Onset Muscle Soreness (DOMS)

Start date: January 2011
Phase: N/A
Study type: Interventional

The study is a single-center, double blinded, randomized controlled trial aimed to investigate the effects of focused extracorporeal shockwave therapy (fESWT) on Delayed Onset Muscle Soreness (DOMS) of the non-dominant biceps brachialis muscle in healthy voluntary adults.

NCT ID: NCT02519387 Completed - Clinical trials for Rheumatoid Arthritis

Efficacy and Safety of Buprenorphine Transdermal Patch in Non-cancer Pain of Moderate Intensity

Start date: July 2013
Phase: Phase 4
Study type: Interventional

This is a phase IV, open-label and single-arm study of patients with non-malignant pain due to osteoarthritis, rheumatoid arthritis, low back pain and joint/muscle pain, who were not responding to non-opioid analgesics. The primary objective was to assess the efficacy of buprenorphine transdermal patch for pain control among these patients.

NCT ID: NCT02481193 Completed - Fasciculation Clinical Trials

Effects of Cisatracurium on Succinylcholine-induced Fasciculations and Myalgia

Start date: March 2013
Phase: Phase 3
Study type: Interventional

The purpose of this study is to investigate the effects of different doses of cisatracurium pretreatment on succinylcholine-induced fasciculations and postoperative myalgia.