Comparison between plain bupivacaine, bupivacaine with nalbuphine and bupivacaine with buprenorphine in spinal anaesthesia
Not Applicable
- Conditions
- Health Condition 1: O- Medical and Surgical
- Registration Number
- CTRI/2022/02/040260
- Lead Sponsor
- DR Prem Sagar
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- ot Yet Recruiting
- Sex
- Not specified
- Target Recruitment
- 0
Inclusion Criteria
PATIENTS UNDERGOING ELECTIVE LOWERLIMB SURGERIES.
AMERICAN SOCIETY OF ANAESTHESIOLOGIST(ASA) GRADE I & II.
Exclusion Criteria
PREGNANCY.
PATIENTS WITH ALLERGY TO DRUG UNDER STUDY.
PATIENTS WITH SPINAL DEFORMITIES.
SUBJECTS HAVING CONTRAINDICATIONS FOR SPINAL ANAESTHESIA
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method To Study The Onset , Duration Of Sensory And Motor Blockade And Any Adverse Effects Of The Given Drug Intrathecally. <br/ ><br>Timepoint: To Study The Onset , Duration Of Sensory And Motor Blockade And Any Adverse Effects Of The Given Drug Intrathecally. <br/ ><br>
- Secondary Outcome Measures
Name Time Method To Study Any Adverse Effects Of Drugs In Post-Operative PeriodTimepoint: From The Time Of Injection to 24Hours Of Time