Randomised control study using Diclofenac patch
Not Applicable
- Conditions
- Health Condition 1: O269- Pregnancy related conditions, unspecified
- Registration Number
- CTRI/2022/12/048088
- Lead Sponsor
- Director USM KLE IMP
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- ot Yet Recruiting
- Sex
- Not specified
- Target Recruitment
- 0
Inclusion Criteria
All pregnant women undergoing Lower Segment Caesarian Section in the age range of 18 to 40 years healthy normal pregnancy completed 38 weeks duration no or mild systemic diseases satisfying to American Society of Anesthesiologists Group I and II who are willing to participate are included in the study
Exclusion Criteria
Patients unsuitable for spinal anaesthesia, history of allergy to analgesic drugs, women with bowel disorders like ulcers inflammatory bowel disease ASA group III and IV and not willing to participate were excluded from the study
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Visual analogue scale score <br/ ><br> No Pain Satisfactory post operation analgesiaTimepoint: at four hours after Caesarian delivery and there after interval of four hours for 48 hours
- Secondary Outcome Measures
Name Time Method The first four post operation days following Caesarian delivery pain free, visual analogue score 1-3 mmTimepoint: Following caesarian delivery mothers do feel pain free at third and fourth days