Buprenorphine as an adjuvant to levobupivacaine in lumbar plexus block for postoperative pain relief after hip, thigh and knee surgeries
Not Applicable
Completed
- Conditions
- Health Condition 1: null- Patients posted for hip & thigh surgeries under spinal Anesthesia having ASA Grade I & II
- Registration Number
- CTRI/2018/01/011437
- Lead Sponsor
- Dr RPGMC Kangra at Tanda
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Completed
- Sex
- Not specified
- Target Recruitment
- 90
Inclusion Criteria
1. scheduled for hip, thigh and knee surgery under subarachnoid block.
2. ASA class I-II.
3. BMI 18.5-29.9.
Exclusion Criteria
1. Patientâ??s refusal either for spinal anesthesia or for lumbar plexus block.
2. Patients with anatomical deformities.
3. Patients having bleeding disorders.
4. Patients with local infection at the sites where needle for spinal and lumbar plexus block is to be inserted.
5. Patients having dysrhythmias on the ECG
6. Patients allergic to study drugs.
7. Patients who are opioid tolerant or opioid dependent.
8. Patients on anticoagulants.
9. Failure of spinal anesthesia.
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method To study and compare post-operative analgesia with two different doses of buprenorphineTimepoint: 24 hours
- Secondary Outcome Measures
Name Time Method Duration of analgesiaTimepoint: 24 hours;Modified Ramsay Sedation ScoreTimepoint: 24 hours;Nausea and VomitingTimepoint: 24 hours;Patient Satisfaction ScoreTimepoint: 24 hours