Comparison of Trigger Point Release Technique of Repetitive Needling with Local Anaesthetic agent versus Local Anaesthetic agent plus Steroid in patients with Myofascial Pain Syndrome.
Phase 3
- Conditions
- Health Condition 1: M791- Myalgia
- Registration Number
- CTRI/2024/05/066716
- Lead Sponsor
- I
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- ot Yet Recruiting
- Sex
- Not specified
- Target Recruitment
- 0
Inclusion Criteria
Patients diagnosed with Myofascial trigger points of any duration.
FaileConservative trial of management tried for at least1 week.
Exclusion Criteria
Not provided
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method pain scores measured by the visual analogue scale (VAS) in which 0 indicated no pain and 10 indicated the most intense pain imaginable.Timepoint: Baseline 2 weeks and 6 weeks
- Secondary Outcome Measures
Name Time Method Quality of Life Assessment using WHO Bref questieneirTimepoint: WHO Bref questioneir will be assessed before the procedure and 6 weeks after the procedure.