A Comparative Study Of Analgesic Effect Of Intrathecal Nalbuphine And Fentanyl As An Adjuvant In Lower Abdomen And Lower Limb Surgery.
Not Applicable
- Conditions
- Health Condition 1: S978- Crushing injury of footHealth Condition 2: S880- Traumatic amputation at knee levelHealth Condition 3: S880- Traumatic amputation at knee level
- Registration Number
- CTRI/2021/11/037720
- Lead Sponsor
- IMS BHU VARANASI
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- ot Yet Recruiting
- Sex
- Not specified
- Target Recruitment
- 0
Inclusion Criteria
Age group between18-65 years,height between160+-10cm,weight between50-75kg,ASA I and II Status,expected to take time of 120-150 minutes
Exclusion Criteria
Patient refusal,patient on beta blocker therapy,ASA III and IV,Patient with known to hypersensitivity to any of the study drugs,pregnancy and patient on sedatives and tranquilizer.
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method evel of sensory block and pain reliefTimepoint: 5 ,15,30,60,120,360,1440 minutes <br/ ><br>
- Secondary Outcome Measures
Name Time Method Full recovery of sensory blockTimepoint: Hours 6 and 12