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Trigger Point Pain, Myofascial clinical trials

View clinical trials related to Trigger Point Pain, Myofascial.

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NCT ID: NCT04316793 Completed - Clinical trials for Trigger Point Pain, Myofascial

Effects of Dry Needling When Applied to the Infraspinatus Muscle in People With Chronic Shoulder Pain

Start date: March 3, 2019
Phase: N/A
Study type: Interventional

Up to 77% of patients with chronic shoulder pain have a trigger point (TrP) in the infraspinatus muscle. These TrPs can lead to pain, limitation of activities and reduced quality of life. Dry needling (DN) is gaining popularity as a treatment for TrPs in physiotherapy. However, its clinical effects remain poorly understood mechanistically and its neurophysiological effects little studied. The primary objective of this study is to determine the feasibility of a larger scale study. The secondary objective of this study is to to explore the immediate neurophysiological, biomechanical and clinical effects of DN and sham needling when applied to TrP of the infraspinatus muscle in people with chronic non-traumatic shoulder pain.

NCT ID: NCT04285216 Completed - Clinical trials for Trigger Point Pain, Myofascial

Effects of Dry Needling and Strain Counter Strain Technique in Myofascial Trigger Points of Upper Trapezius

Start date: September 15, 2019
Phase: N/A
Study type: Interventional

To determine the effects of Dry Needling and Strain Counter Strain Technique in Myofascial Trigger Points of Upper Trapezius

NCT ID: NCT04267315 Active, not recruiting - Breast Cancer Clinical Trials

Trigger Point Injections for Post-Mastectomy Pain Syndrome

Start date: January 3, 2020
Phase: Phase 2
Study type: Interventional

Post-Mastectomy Pain Syndrome (PMPS) is a chronic pain that persists for more than three months after a surgical breast procedure. It has 11-70% incidence in patients that underwent a breast surgery. It consists of mixed pain, frequently associated with myofascial pain, an specific type of muscular pain. Trigger point injections (TPI) are classically used for the treatment of myofascial pain in other painful conditions. However, there are no controlled trials assessing the efficacy of TPI in the treatment of PMPS. The intervention objective is to assess the efficacy of TPI in patients with PMPS, when associated with a comprehensive rehabilitation program and pain management.

NCT ID: NCT04157439 Completed - Clinical trials for Trigger Point Pain, Myofascial

Manual Treatment Regimens in Upper Trapezius Trigger Point

Start date: September 8, 2018
Phase: N/A
Study type: Interventional

To compare the effect of sustain pressure and Integrated Neuromuscular Inhibition Technique on individuals with upper trapezius Trigger points (TrPs). The Study Design was Randomized control trial. According to inclusive criteria 26 patients were randomly allocated by sealed envelope method in experimental and control group. Patients were assessed at baseline and 4th day of session on NPRS, NDI questionnaire and ranges were taken by Goniometer and pressure threshold by Algometer. There was 3 drop out and the reason was loss of follow up. Hot pack was applied to both groups for 10mints before session. Sustain pressure was given for 3sec hold and 2sec release till pain decreases in control group. While, in experimental group INIT was used. Sustain pressure was applied on MTrPs for 3sec hold and 2sec release till pain decreases, Post isometric relaxation (MET) was given with 6-10 sec hold and repeat 4 times and at last Strain counter-strain (SCS) was given to hold muscle in shortest position for 90sec or pain reduced to 3 out of 10. At last cervical stretches were given and home plan was guided.

NCT ID: NCT04157426 Completed - Clinical trials for Trigger Point Pain, Myofascial

Percutaneous Electrolysis Versus Dry Needling in Levator Scapulae

Start date: September 28, 2021
Phase: N/A
Study type: Interventional

The objective will be to determine the effectiveness of ultrasound-guided percutaneous electrolysis versus ultrasound-guided dry needling in active myofascial trigger points of the levator scapulae muscle on pain intensity, disability and range of motion. A randomized clinical trial will be carried out. Fifty-four patients with at least one active myofascial trigger point in the levator scapulae muscle were recruited and divided into ultrasound-guided percutaneous electrolysis (n = 27) and ultrasound-guided dry needling (n=27). Pain intensity, disability and range of motion will measured before, immediately after and 1 week after intervention.

NCT ID: NCT04136197 Completed - Clinical trials for Trigger Point Pain, Myofascial

Trigger Point Incidence After Lumbar Disc Herniation Surgery

Start date: July 18, 2020
Phase:
Study type: Observational

Our purpose is to determine the incidence of trigger points in patients who remain in a fixed position for a long time during lumbar disc herniation surgery.

NCT ID: NCT04108390 Active, not recruiting - Clinical trials for Trigger Point Pain, Myofascial

Gluteus Medius Dry Needling and Ankle Instability

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

Randomized clinical trial in individuals with chronic ankle instability. Main outcomes were as follows: pain intensity, pressure pain threshold, lower limb balance and range of motion. The sample will be divided in two groups: 1) dry needling at the gluteus medius trigger point (intervention). 2) dry needling 1,5 cm from the gluteus medius trigger point (control).

NCT ID: NCT04066166 Completed - Clinical trials for Trigger Point Pain, Myofascial

Accuracy of Rib Palpation for Dry Needling of Deep Periscapular Musculature, Measured With Ultrasound

Start date: January 1, 2016
Phase:
Study type: Observational

Ultrasound was used to identify the location of a rib. This was compared to a practitioner's ability to palpate the area.

NCT ID: NCT03888586 Completed - Clinical trials for Subacromial Impingement Syndrome

Comparison of Dry Needling and Deep Friction Massage in Patients With Subacromial Pain Syndrome

Dry Needling
Start date: October 2, 2017
Phase: N/A
Study type: Interventional

This study was planned to investigate the effects of Trigger Point-Dry Needling Therapy (TP-DNT) on night pain and Shoulder Internal Rotation (SIR) in individuals with Subacromial Pain Syndrome (SPS).

NCT ID: NCT03870191 Completed - Nerve Block Clinical Trials

Comparison of Therapeutic Effects of Trigger Point Injection and Twin Nerve Block in Chronic Myofascial Pain Patients

Start date: June 21, 2016
Phase: N/A
Study type: Interventional

To see if there is there any difference in the treatment outcomes/results such as changes in pain intensity in patients with myofascial pain who have been treated with trigger point injections or twin block?