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Myofascial Pain Syndrome clinical trials

View clinical trials related to Myofascial Pain Syndrome.

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NCT ID: NCT04998630 Recruiting - Clinical trials for Myofascial Pain Syndrome

Comparison of Focused ESWT by Frequency for Patients With Myofascial Pain Syndrome

Start date: June 22, 2021
Phase: N/A
Study type: Interventional

To investigate the efficacy and safety according to the frequency of focused ESWT in patients with myofascial pain syndrome.

NCT ID: NCT04904367 Completed - Clinical trials for Myofascial Pain Syndrome

Deep Tissue Massage in the Myofascial Pain Syndrome

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

This study aims to examine the effect of deep tissue massage (DTM) on myofascial trigger point (MTrP) number, neck range of motion (ROM), pain, disability and quality of life in patients with Myofacial pain syndrome (MPS).

NCT ID: NCT04900857 Completed - Clinical trials for Myofascial Pain Syndrome

Comparison of Vibration and Dry Needle in Trigger Point Therapy

Start date: December 7, 2020
Phase: N/A
Study type: Interventional

The aim of this study is to compare the effects of localized vibration and dry needling applied to the trigger point in the individuals with acute myofascial pain syndrome.Pressure pain threshold (PPT) was used for the primary outcome measure of the study, and pain intensity, pain tolerance and short form (SF-36) were used for secondary outcome measures.

NCT ID: NCT04885881 Completed - Clinical trials for Myofascial Pain Syndrome

The Effectiveness of Ozone (O2-O3) Injections in the Treatment of Myofascial Pain Syndrome

Start date: April 15, 2021
Phase: N/A
Study type: Interventional

Ozone (O2-O3) has been used as a supportive therapy in various musculoskeletal diseases such as lumbosacral disc herniation, knee osteoarthritis, meniscus injury, shoulder pathologies.The aim of this study is to investigate the effectiveness of ozone (O2-O3) injection applied to the trigger point in the treatment of myofascial pain syndrome.

NCT ID: NCT04832074 Completed - Neck Pain Clinical Trials

Immediate Stiffness Changes in Myofascial Trigger Points After Dry Needling

ELECTROP
Start date: May 5, 2021
Phase: N/A
Study type: Interventional

Shear-wave elastography (SWE) is considered as a useful tool for quantifying muscle stiffness. Considering that Myofascial Trigger Points (MTrP) are defined as "hyperirritable zones in contracted bands of muscle, thought to be caused by muscle overload or stress" and the effectiveness of dry needling applied to active MTrP for reducing pain and disability, the aim of this study is to assess the effects of sham and real dry needling, applied to active MTrP in the upper trapezius muscle in patients with chronic neck pain, on the muscle stiffness in two areas: 1) the most symptomatic area and 2) a control point.

NCT ID: NCT04814017 Completed - Chronic Pain Clinical Trials

Effectiveness of Shock-wave Therapy in Patients With Myofascial Pain Syndrome

Start date: January 28, 2013
Phase: N/A
Study type: Interventional

30 patients with chronic cervical myofascial pain (4 males, 26 females) aged between 25 to 57 years (with average age 41,20±10,23 years) were included the study. Participants were divided into two groups as intervention group (n=15) and control group (n=15). Patients in intervention group received radial shock-wave application one times a week for six weeks and home based stretching exercises. Patients in control group (CG) received home based stretching exercises. Rest and activity pain (Visual Analog Scale), pressure pain threshold (PPT), cervical range of motion (CROM) and disability (Neck Disability Index) were assessed at baseline and after the treatment.

NCT ID: NCT04789811 Enrolling by invitation - Clinical trials for Myofascial Pain Syndrome

Exercise and Dry Needling Treatment Combination in Nocturnal Calf Cramps

Start date: December 1, 2020
Phase: N/A
Study type: Interventional

The Investigators aim to evaluate the effectiveness of dry needling treatment in addition to stretching exercises on cramp duration, cramp intensity, cramp frequency, sleep quality, and sensitivity of myofascial trigger points in patients with nocturnal calf cramp.

NCT ID: NCT04751110 Completed - Clinical trials for Myofascial Pain Syndrome

Ultrasound Guided Rhomboid Intercostal Block for Myofascial Pain Syndrome

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

Rhomboid intercostal block (RIB) is an interfacial plane block described in 2016. It creates analgesia at T2-T9 levels in the hemithorax by applying local anesthetic to the fascia between the rhomboid muscle and the intercostal muscle. It has been used effectively in patients with chronic pain. Recently published report has shown that rhomboid intercostal block (RIB) may provide effective pain control for myofascial pain syndrome (MPS), too. MPS is a regional pain syndrome characterized by trigger points detected in one or more regional muscle groups. The investigators planned a prospective observational study, a total of 30 patients who will apply to our clinic with MPS, will register in research. The investigators will perform ultrasound-guided RIB, and evaluate the clinical outcomes.

NCT ID: NCT04640558 Completed - Muscle Weakness Clinical Trials

Gluteus Medius Latent Trigger Point and Muscle Strength in Healthy Subjects

Start date: November 17, 2020
Phase:
Study type: Observational [Patient Registry]

This study aimed to investigate the relationship between latent MTrPs and gluteus medius muscle strength in a group of healthy adults.

NCT ID: NCT04628312 Completed - Clinical trials for Myofascial Pain Syndrome

Foot Plantar Pressure Changes After Plantar Dry Needling

Start date: November 20, 2020
Phase: N/A
Study type: Interventional

The aim of this clinical trial is to check the effects of dry needling in the Flexor digitorum Brevis. Twenty healthy subjects wil be recruited for a quasi-experimental study. Participants will be from 18 to 40 years old, not obese. Participants will be measured before and after bilateral dry neddling in Flexor digitorum Brevis. The investigators will measure static footprint variables. The footprint variables will be divided in bilateral rear foot, bilateral midfoot, bilateral fore foot.