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Myofascial Pain Syndrome clinical trials

View clinical trials related to Myofascial Pain Syndrome.

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NCT ID: NCT05318560 Not yet recruiting - Clinical trials for Myofascial Pain Syndrome

Efficacy of Local Anesthetic and Ozone Injection in Patients With Myofascial Pain Syndrome

Start date: June 30, 2022
Phase: N/A
Study type: Interventional

In this study, the investigators planned to compare local anesthetic injection added to stretching exercise, ozone injection treatment added to stretching exercise, and only stretching exercise in patients with upper trapezius muscle myofascial pain syndrome.

NCT ID: NCT05265884 Recruiting - Clinical trials for Myofascial Pain Syndrome

Effect of Kinesiotaping on Myofascial Pain Syndrome Post Neck Dissection Surgery

Start date: March 1, 2022
Phase: N/A
Study type: Interventional

The purpose of the study is to evaluate the effect of Kinesio taping on myofascial pain syndrome post neck dissection surgery.

NCT ID: NCT05225571 Completed - Neck Pain Clinical Trials

The Relationship of Cervical Sagittal Parameters With Pain and Disability in Cervical Myofascial Pain Syndrome

Start date: September 1, 2021
Phase:
Study type: Observational [Patient Registry]

Participants between the ages of 18-64 who were diagnosed with cervical myofascial pain syndrome will be included in the study. cervical sagittal parameters, numerical pain rating scale, Bournemouth neck questionnaire and cervical range of motion will be measured and evaluated.

NCT ID: NCT05187468 Completed - Clinical trials for Myofascial Pain Syndrome

The Effectiveness of Radial ESWT on Upper Trapezius Mtrps

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

This study looked after the effectiveness of radial ESWT on upper trapezius mtrps. There were three intervention groups which recieved either ESWT or standard care. VAS, PPT, Neck ROM and Cervical functionality were the main outcomes.

NCT ID: NCT05185050 Completed - Clinical trials for Myofascial Pain Syndrome

Prevalence of Myofascial Pain Syndrome in Adolescent Idiopathic Scoliosis

Start date: October 10, 2021
Phase:
Study type: Observational [Patient Registry]

this is an observational and cross-sectional prevalence study. 10-18 years aged participants with adolescent idiopathic scoliosis were recruited in the study. Myofascial pain syndrome will be questioned to the participants. additionally, all participants will be evaluated using their findings for scoliosis and myofascial pain syndrome diagnostic criteria. Cobb angle, coronal balance, shoulder and pelvis asymmetry, sagittal spino-pelvic parameters of the spine (cervical lordosis, thoracic kyphosis, lumbar lordosis angles and sagittal vertical axis, sacral slop angle and pelvic incidence) will be measured.

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.

NCT ID: NCT05073900 Completed - Clinical trials for Myofascial Pain Syndrome

Comparison of the Efficacy of Rhomboid Intercostal Block and Erector Spinal Plane Block on Myofascial Pain Syndrome

Start date: July 10, 2021
Phase: N/A
Study type: Interventional

The investigators evaluate the effect of Ultrasound guided Rhomboid Intercostal Block and Erector Spinal Plane Block on lower cervical and inter scapular Myofascial Pain

NCT ID: NCT05030181 Completed - Pain Clinical Trials

Efficacy of Kinesiology Tape on Neck Disability

Start date: April 1, 2021
Phase: N/A
Study type: Interventional

Sixty participants with nonspecific neck pain were randomly assigned to either the kinesiotaping (n=30) or exercise (n=30) group. At the beginning, at the 2nd week and at the 1st month, activity and rest pain with visual analog scale, cervical lateral flexion and rotation with goniometer, neck disability scale and trapezius thickness, trigger point volume, trigger point diameter, trigger point area (with ultrasonograpic imaging) will be evaluated. After the initial evaluation of the patients in the kinesiotaping group, 'I' strip kinesiotape will be applied with the space correction technique for the upper trapezius muscle, for a total of 4 sessions, 2 days a week, and the patients will be included in the 1-month home exercise program. Patients will be evaluated at the start of treatment, Week 2, and Month. Patients in the control group will only be included in the 1-month home exercise program. Patients will be evaluated at the start of treatment, Week 2, and Month 1. The participants inclusion criteria were; age between 18 and 65 years, symptom duration of at least 3 months. The exclusion criteria were as follows: (1) a diagnosis of cervical radiculopathy or myelopathy, (2) a history of acute neck injury or cervical surgery (3) diagnosis of psychiatric disorders (4) recent trigger-point injection or participation in a physical treatment program witin the last 6 monhts (5) any allergies to the tape and (6) having already received treatment with kinesio-taping.

NCT ID: NCT05022888 Not yet recruiting - Clinical trials for Myofascial Pain Syndrome

Near-Infrared Spectroscopy in Myofascial Pain Syndrome

Start date: August 23, 2021
Phase: N/A
Study type: Interventional

Myofascial pain syndrome is a regional pain syndrome accompanied by sensorial, motor and autonomic symptoms . myofascial trigger points are most frequently detected in the upper trapezius, levator scapula, and axial postural muscles such as rhomboid major. Myofascial pain syndrome is characterized by active myofascial trigger points in the form of focal hyperirritable nodules palpated in the tight band of the muscle . Alteration of tissue vascularization could limit or prevent th may cause adhesions, contractures and pain. As a result of decreased blood flow, tissue oxygenation may decrease.

NCT ID: NCT05009264 Completed - Clinical trials for Myofascial Pain Syndrome

OMTrigger Inject- Treating Trigger Points: Comparing Muscle Energy Technique vs. Lidocaine Needling Technique

Start date: January 12, 2022
Phase:
Study type: Observational

The primary aim of this study is to determine if osteopathic manipulative treatment is as effective to traditional lidocaine injection technique in treating myofascial trigger points in regard to post intervention pain intensity and quality of life.