Clinical Trials Logo

Myofacial Pain clinical trials

View clinical trials related to Myofacial Pain.

Filter by:

NCT ID: NCT06358326 Recruiting - Clinical trials for Carpal Tunnel Syndrome

Dry Needling and Rehabilitatin Carpal Tunnel Syndrome

Start date: April 5, 2024
Phase: N/A
Study type: Interventional

Dry needling is used for myofascial release. However, its effectiveness in carpal tunnel syndrome (CTS) is not well known. It is thought that dry needling may also be an effective treatment for CTS by providing relaxation in the fascial tissue. Therefore, this study will examine the effects of dry needling treatment on pain, function, range of motion, proprioception and disability in patients with CTS.

NCT ID: NCT06051799 Recruiting - Clinical trials for Trigger Point Pain, Myofascial

Effects of Pressure Release of Myofascial Trigger Points on Mechanical Neck Pain.

Start date: September 25, 2023
Phase: N/A
Study type: Interventional

The study aims to compare the effectiveness of myofascial trigger point treatment using pressure release versus a control group in patients with mechanical neck pain, randomly assigned. In both groups a protocol of therapeutic exercise and postural correction will be carried out

NCT ID: NCT05673655 Enrolling by invitation - Myofacial Pain Clinical Trials

Intraoral Injection of Trigger Points by Botox

Start date: December 25, 2022
Phase: Phase 2
Study type: Interventional

Patients with orofacial pain lasting at least 3 months. The patients will be randomly assigned to one of the two groups according to the treatment method: group I (intraoral injection) and group II (transcutaneous injection) where each patient injected Botox at each trigger point according to the treatment group by the same operator. Patients will be examined by a blinded investigator at pre- and post-injections at the following intervals: during diagnosis, 1 week, 4, and 6 weeks post-injection. The patients will be assessed using a pain score measured on a 10-point visual analog scale (VAS). The secondary outcome assessed will be measuring the quality of life in an Oral Health Impact Profile questionnaire (OHIP-14).

NCT ID: NCT05619380 Recruiting - Pain Clinical Trials

Effectiveness of Physiotherapy Treatments in Temporomandibular Joint Dysfunction

Start date: November 20, 2022
Phase: N/A
Study type: Interventional

The study will determinate the influence of four selected physiotherapeutic procedures on the pain intensity, the bioelectrical activity of the masseter muscle, and the range of mandibular mobility in patients with TMDs (temporomandibular joint dysfunction).

NCT ID: NCT05358730 Completed - Pain, Shoulder Clinical Trials

Effects of IASTM in the Treatment of Adhesive Capsulitis

Start date: March 10, 2019
Phase: N/A
Study type: Interventional

This study aimed to determine the effects of IASTM in combination with exercise in frozen shoulder. Thirty-five patients with phase II frozen shoulder included in this single-blind, randomized study. Patients were divided into two groups. In the first group exercise programme (Group 1) and in the second group IASTM in combination with exercise programme (Group 2) were applied for twelve sessions (two days per week for six week). The primary outcome was the Disabilities of the Arm, Shoulder and Hand (DASH) score and secondary outcomes were the visual analogue scale (VAS), the range of motion (ROM), The Constant score and Short- Form-36 (SF-36). Outcome measures were performed at baseline, after the 6th session and the 12th session.

NCT ID: NCT05228327 Completed - Myofacial Pain Clinical Trials

Occlusal Splint and Masticatory Muscle Injection in Myofacial Pain

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

Myofascial pain is one of the common symptoms in patients with temporomandibular joint disorders. Occlusal splint use, trigger point injections and the combination of this two methods are primary treatment options. Patients were divided into 3 groups and this three treatment was applied. We aimed to investigate the clinical and ultrasonographic effects of the treatments. Patients in the treatment groups were reexamined at 1st and 3rd months, and their clinic and ultrasonographic records were repeated. 16 healthy volunteers were also included in the study. No treatment was applied, only clinical and ultrasonographic records were taken once.

NCT ID: NCT05151510 Recruiting - Clinical trials for Myofascial Trigger Point Pain

Trigger Point Injections Versus Lidocaine Patch for Myofascial Pain in the Emergency Department

Start date: November 1, 2021
Phase: Phase 4
Study type: Interventional

The aim of this trial is to investigate the efficacy of trigger point injections with 1% lidocaine in reducing myofascial back and neck pain in the Emergency Department compared to lidocaine patches 5%.

NCT ID: NCT04640896 Recruiting - Pain, Back Clinical Trials

Trigger Point Injections in Anterior Cervical Surgery

Start date: November 5, 2020
Phase: Phase 4
Study type: Interventional

To achieve appropriate exposure for an anterior neck surgery (for example an Anterior Cervical Discectomy and Fusion or ACDF), patients are positioned supine with their neck extended. Due to being in this position, patients frequently complain of posterior neck stiffness and pain postoperatively in addition to the anterior incisional pain. This posterior cervical pain can be classified as myofascial pain. Cervical myofascial pain is thought to be the result of overuse or trauma to the supporting muscles of the neck and shoulders. Trigger point injections are one of the methods used to treat myofascial pain. The trigger point injection procedure is where a physician (typically an anesthesiologist) performs an exam of the patient neck and upper back and finds areas of point tenderness. The physician will then inject a small amount of numbing medication (such as bupivacaine) into the muscle or tissue in that area. Trigger point injections have been shown to be superior to botox injections or dry needling, and equivalent to physical therapy. However, these studies were performed on patients with chronic neck pain. There are no studies evaluating the effectiveness of trigger point injections on post anterior cervical surgery patients. At our institution, trigger point injections with local anesthetic are used as part of a multimodal pain control regimen for post-anterior cervical surgery patients. Our hypothesis is if the addition of trigger point injections to standard of care multi-modal post-operative pain control will decrease patients' myofascial pain, and thereby decrease the amount of narcotic pain medication used.

NCT ID: NCT04568915 Completed - Neck Pain Clinical Trials

Dry Needling and Maitland Joint Mobilization Techniques in Patients With Myofacial Chronic Neck Pain

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

The purpose of my research is to compare the effects of dry needling and Maitland mobilization in chronic myofacial neck pain

NCT ID: NCT04298554 Completed - TMD Clinical Trials

Comparison of Cannabinoids to Placebo in Management of TMJ Pain and Myofascial Pain in the TMJ Region

Start date: August 6, 2020
Phase: N/A
Study type: Interventional

The aim of this study is to determine whether the cannabinoids taken orally in the form of cannabidiol (CBD oil-a major non-psychoactive component of marijuana) vs placebo (hemp oil) will provide pain relief and improved jaw function in those who suffer from either myofascial pain disorder and/or arthralgia of the temporomandibular region. 1. Primary Objectives To determine if the consumption of CBD oil is superior to placebo for the improvement in jaw pain. 2. Secondary Objectives To determine if the consumption of CBD oil is superior to placebo for the improvement in function of the temporomandibular joint. 3. Exploratory Objectives To determine if there are any adverse effects that result from the consumption of CBD oil or placebo.