The analgesic efficiency of nerve block for abdominal surgery.A prospective randomised control study.
Not Applicable
- Conditions
- Health Condition 1: N879- Dysplasia of cervix uteri, unspecified
- Registration Number
- CTRI/2020/06/025580
- Lead Sponsor
- IGIIMS
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- ot Yet Recruiting
- Sex
- Not specified
- Target Recruitment
- 0
Inclusion Criteria
Patients of either sex aged between 20 - 50 yrs.
Patients posted for open abdominal surgery under general anaesthesia
ASA physical status 1&2
Exclusion Criteria
Patient refusal.
Patient with allergy to study drugs
Patient with co-morbidities such as diabetes, hypertension etc.
coagulopathy
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method post operative anagesiaTimepoint: post operative anagesia
- Secondary Outcome Measures
Name Time Method adverse effeect like hypotention,bradycardiaTimepoint: post operative period