Comparison of safety of transdermal ketoprofen and diclofenac patches in post-operative pain management
Phase 4
- Conditions
- Health Condition 1: - Health Condition 2: O- Medical and Surgical
- Registration Number
- CTRI/2024/01/061659
- Lead Sponsor
- Sri Lalithambigai medical college
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- ot Yet Recruiting
- Sex
- Not specified
- Target Recruitment
- 0
Inclusion Criteria
who were all undergoing lower limb surgeries (ORIF).
Exclusion Criteria
pregnant or lactating mothers, patients on chronic pain treatment, patients with known allergy to the study drug, with any bleeding disorders, with history of impaired cognitive functions and history of alcohol and substance abuse.
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method postoperative pain was taken in a visual analogue scaleTimepoint: visual analogue scale (VAS) were used. VAS score was recorded at 4,6,8,12 and 24 hours postoperatively
- Secondary Outcome Measures
Name Time Method Sleep interference score was also recorded on a 10-point scaleTimepoint: how the pain had interfered with patient’s sleep during the first 24 hours