comparison of two doses of buprenorphine as spinal Adjuvant to 0.5% Bupivacaine for adult patients undergoing lower limb orthopedic surgeries
Phase 1
- Conditions
- Health Condition 1: M849- Disorder of continuity of bone, unspecified
- Registration Number
- CTRI/2024/04/065175
- Lead Sponsor
- Mahatma Gandhi Institute of Medical Sciences kasturba hospital
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- ot Yet Recruiting
- Sex
- Not specified
- Target Recruitment
- 0
Inclusion Criteria
. American Society of Anesthesiologists Grade I and II patients.
. Adult patients aged more than 18 years of either gender.
. Patients undergoing lower limb orthopedic surgeries.
. Height is more than 4 feet.
Exclusion Criteria
. American Society of Anesthesiologist Grade III and IV patients.
. Patients with known contraindications for spinal anesthesia: bleeding disorders, local
Infection.
. Patients with hemodynamic instability.
. Patients with allergy to or history of hypersensitivity to local anesthetics.
. Emergency surgeries.
. Patients with known allergy to opioids.
.Patients refusal.
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method inreased duration of sensory & motor blockadeTimepoint: 15min 30min 45min
- Secondary Outcome Measures
Name Time Method onset & level of sensory and motor blockade achievedTimepoint: 15min 30min 45min