A study for the comperison of pain-free duration after administration of inj.butorphenal vs inj.fentanyl with inj.levobupivacaine epidurally in patients undergoing vaginal hysterectomy
Not Applicable
- Conditions
- Health Condition 1: N819- Female genital prolapse, unspecifiedHealth Condition 2: 1- Obstetrics
- Registration Number
- CTRI/2023/12/060886
- Lead Sponsor
- JLN medical college
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- ot Yet Recruiting
- Sex
- Not specified
- Target Recruitment
- 0
Inclusion Criteria
ASA 1 and 2
female undergoing vaginal hysterectomy
Exclusion Criteria
ASA >2
comorbidities
pregnant patients
breastfeeding
local infection
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method
- Secondary Outcome Measures
Name Time Method