A Study On Effectiveness Of Paracervical Block and Requirement of Additional Analgesia
Phase 3
- Conditions
- Health Condition 1: O- Medical and Surgical
- Registration Number
- CTRI/2023/11/059924
- Lead Sponsor
- Shimoga Institute Of Medical Sciences
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- ot Yet Recruiting
- Sex
- Not specified
- Target Recruitment
- 0
Inclusion Criteria
Peri and post menpausal age group
ASA II III catagories
Exclusion Criteria
ASA I
Allergy to local anaesthetic
Infection at the site of injection
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Effectiveness of paracervical blockTimepoint: vas score 5, from baseline to 20mins
- Secondary Outcome Measures
Name Time Method eed for additional analgesia & sedation along with the blockTimepoint: vas score 5 from baseline to 20mins