Compare Nalbuphine and Buprenorphine in spinal anaesthesia for post operative pain relief.
Phase 3
Completed
- Conditions
- Health Condition 1: O- Medical and Surgical
- Registration Number
- CTRI/2021/01/030672
- Lead Sponsor
- university college of medical sciences and GTB hospital
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Completed
- Sex
- Not specified
- Target Recruitment
- 46
Inclusion Criteria
Patients belonging to ASA grade 1 and 2 who are undergoing orthopedic lower limb surgery with height >150cm and <180cm.
Exclusion Criteria
Patients with contraindication to spinal anaesthesia of body weight >120kg with known allergy to study drug.
Patient with history of chronic pain or long term opioid use.
Patient refusal.
Multiple fractures preventing proper assessment of anaesthesia.
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Duration of post operative analgesia.Timepoint: pain will be assessed every 30 minutes for first 2 hours, at 4th, 8th, 12th and 24th hour respectively.
- Secondary Outcome Measures
Name Time Method Post operative pain assessment and total analgesic requirement.Timepoint: For 24 hours.;Time of onset, intensity and duration of mootor block.Timepoint: onset is time taken to reach modified bromage grade 3. <br/ ><br>Duraton is time taken to reach modified bromage grade 0.;Time of onset, maximum level, time to achieve maximum level and duration of sensory block.Timepoint: onset is time taken for block to reach T10 segment.