A study to compare the effectiveness of two different types of painkiller topical formulations
Phase 4
Completed
- Conditions
- Health Condition 1: null- Patients suffering from acute musculoskeletalpainful conditions
- Registration Number
- CTRI/2018/04/013316
- Lead Sponsor
- Armed Forces Medical College Pune
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Completed
- Sex
- Not specified
- Target Recruitment
- 140
Inclusion Criteria
All adult patients with acute painful musculoskeletal pain
Exclusion Criteria
1. All patients denying consent to participate in the trial
2. All patients with deep abrasions and lacerations around the area of affliction
3. Individuals with known adverse reaction to topical Diclofenac preparations.
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Pain intensity difference (PID) from baseline (before starting treatment) during movement (of affected area) and at restTimepoint: Day 3 and 7
- Secondary Outcome Measures
Name Time Method 1.Requirement of oral analgesics <br/ ><br>2. Side effectsTimepoint: Day 3 and 7