A study to see the effect of dry needling for pain relief in patient suffering from myofascial pain and who already undergone spinal operation.
Not Applicable
- Conditions
- Health Condition 1: M961- Postlaminectomy syndrome, not elsewhere classified
- Registration Number
- CTRI/2018/04/013107
- Lead Sponsor
- ESI Institute of Pain Management ESI Hospital Sealdah
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- ot Yet Recruiting
- Sex
- Not specified
- Target Recruitment
- 0
Inclusion Criteria
Patients who had been operated for spinal pathology and having persistent back pain or recurrent back pain for more than six months not responding to conservative treatment with myofascial trigger points.
Exclusion Criteria
Patient having needle phobia or behavioral disorder.
Bleeding disorder or on anticoagulant medication.
Localized or systemic infection.
Red flags sign for spinal pain in FBSS.
FBSS with Radiculopathy.
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method
- Secondary Outcome Measures
Name Time Method