Health Condition 1: M797- Fibromyalgia
Conditions
Interventions
Sponsors
Eligibility
Inclusion criteria
Inclusion criteria: 1.Subjects meeting the criteria of - 2.Subjects with chronic pain � 6 months. 3.Married and living with partner 4.Local tenderness at 12 of 14 specified sites. 5. Disturbed sleep, with morning fatigue and stiffness. 6. Subjects those are willing to discontinue taking all pain relieving medications(analgesics and NSAIDS, except paracetamol upto 4g/day. 7. Normal laboratory findings
Exclusion criteria
Exclusion criteria: 1.Participant Refusal 2.pregnant women 3. patients with history of a chronic medical conditions like: malignancy, systemic inflammatory disorders. 4.Subjects under treatment of psychiatric conditions and neurological disorders 5. Patients with any history of recent surgery.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| 1. Pain Intensity 2. Tenderness 2. Quality of Life Timepoint: 1. Baseline(Pre-Intervention) 2. Post Intervention-I(After 4 weeks from the baseline study) 3. Post Intervention-II (After 6 weeks from the Post Intervention-I Readings) 4 Follow up (After 2 weeks from Post Intervention-II Readings) | — |
Secondary
| Measure | Time frame |
|---|---|
| Activities of Daily LivingTimepoint: 1. Baseline(Pre-Intervention) 2. Post Intervention-I(After 4 weeks from the baseline study) 3. Post Intervention-II (After 6 weeks from the Post Intervention-I Readings) 4 Follow up (After 2 weeks from Post Intervention-II Readings) | — |
Countries
India
Contacts
Delhi Pharmaceutical Sciences and Research University