Skip to main content
OpenTrials
Completed

NCT Number: NCT03870191

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

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?

Completed

Looking for future studies?

Notify Me

Key information

About this study

Most treatment approaches for chronic myofascial pain are not evidence-based. Studies are usually controversial. Most are short-term, non-randomized. An essential limitation has been the lack of standardization of diagnosis. Some studies do not differentiate between joint pain and muscle pain, which can significantly affect the outcome of the treatment provided.

Diagnostic Criteria for Temporomandibular Disorders (DC/TMD) was recently published and validated. Their protocol allows standardization of the assessment and diagnosis of patients with temporomandibular disorder, including myofascial pain.

To the investigator's knowledge, no previous prospective, randomized study has been conducted demonstrating the treatment outcomes of either trigger point injections or twin block in patients with chronic myofascial pain.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Patients diagnosed with Myofascial pain with referral based on the DC/TMD criteria
  • Pain on the masseter and or temporalis muscles
  • Pain present for at least 3 months

Exclusion criteria

  • Generalized muscle disorder such as fibromyalgia
  • Subjects on chronic pain medication
  • Subjects who are known to have hypersensitivity to the local anesthetics.
  • Pregnant women. A pregnancy test will not be given before subject enrollment. Women of childbearing ages will be asked verbally if they are pregnant. If they are unsure, then they will be excluded from the study.
  • Subjects with cognitive problems e.g. Alzheimer's disease.

Treatment and study plan

Injection of either twin block or trigger point injection.

Other

Study participants will be randomized into either group and will receive the intervention.

Primary outcomes

  1. Pain relief: numerical pain scale

    Time frame: 6 months

    The pain relief received from each injection will be measured using the numerical pain scale. This scale is between 0-10 with 0 meaning no pain and 10 is the most pain.Higher values represent worse pain.

Sponsors and collaborators

Lead sponsor

Rutgers University

Other

Registry information

Important dates

Study start
2016
Primary completion
2018
Study completion
2020
First posted
Mar 12, 2019
Registry last updated
Jun 19, 2020

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

Published trials that share one or more normalized conditions with this study.