A randomized comparative study on rectal versus oral Diclofenac for perineal pain relief following episiotomy repair in a tertiary hospital
Phase 3
- Conditions
- Episiotomy pain
- Registration Number
- PACTR202308864630455
- Lead Sponsor
- Princeba Tamunobelema Amachree
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Pending
- Sex
- Female
- Target Recruitment
- 132
Inclusion Criteria
1. All parturients who will have episiotomy repair following delivery.
2. Live foetuses
3. All booked consenting women whose consent will be revalidated during labou
Exclusion Criteria
1.Women with contraindications to NSAIDS e.g. peptic ulcer, liver disease, renal disease, bronchial asthma.
2. Women who will have 3rd or 4th-degree perineal tear
3. Women with severe primary postpartum haemorrhage >1000mls.
4. Any patient that would require specialized post- delivery pain control such as Sickle cell disease patients
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method
- Secondary Outcome Measures
Name Time Method