The effectiveness of ya-thor-ra-nee-san-tha-kat compare with naproxen tablets for the treatment in chronic Myofascial pain syndrome
Phase 4
Completed
- Conditions
- This study included patients with myofascial pain syndrome,who visited the Internal Medicine Department,Srinagarind Hospital,Faculty of Medicine,Khon Kaen University. Inclusion criteria of the stumyofascial pain syndrome
- Registration Number
- TCTR20190318002
- Lead Sponsor
- Khon Kaen University
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Completed
- Sex
- All
- Target Recruitment
- 82
Inclusion Criteria
adults aged between 25-75 years who had been diagnosed with myofascial pain syndrome affecting both trapezius muscles (at least one active trigger point).
Chronic pain (not less than 3 months) in the neck or shoulder area
Pain score not less than 6 out of 10.
Not undergone other treatments including massage, acupuncture
Not undergone the operation in the muscle area within 1 year prior to this study
No allergy history with NSAIDS or herbal drugs
Exclusion Criteria
Pregnancy
Patients with infectious diseases, tuberculosis, diabetes, cancer hypertension, kidney diseases, liver diseases, epilepsy
handicapped person
paralysis
patients who have muscle pain from other causes including radiculopathy, myelopathy, disc herniation, osteoarthritis
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method umerical pain score 14 days Numeric Pain Rating Scale ,Angle of joint rotation 14 days Cervical range of motion,The minimum pain pressure threshold 14 days Goniometer
- Secondary Outcome Measures
Name Time Method Ceatinine clearance 14 days Clinical blood test,Aspartate Aminotransferase 14 days Clinical blood test,Alanine Aminotransferase 14 days Clinical blood test