A comparative assessment on the effectiveness of paracervical block and rectal diclofenac for pain relief during diagnostic hysteroscopy.
Phase 2
- Conditions
- No
- Registration Number
- PACTR202303663072593
- Lead Sponsor
- Duru Victor Chinazom
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Pending
- Sex
- Female
- Target Recruitment
- 100
Inclusion Criteria
?Women undergoing diagnostic hysteroscopy and gave consent for the study
Exclusion Criteria
1.Women who are allergic to lignocaine/diclofenac
2.Women who had failed attempts at previous hysteroscopy
3.Women with cervicitis or active pelvic inflammatory disease
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method The primary outcome, measured the mean pain scores in the participants who will receive rectal diclofenac or PCB during diagnostic hysteroscopy
- Secondary Outcome Measures
Name Time Method 1.patient satisfaction 2.Side effects during diagnostic hysteroscopy