To compare butorphanol and buprenorphine with levo-bupivacaine for post-operative analgesia
Not Applicable
- Conditions
- Health Condition 1: O- Medical and Surgical
- Registration Number
- CTRI/2023/08/056741
- Lead Sponsor
- Rohilkhand Medical College And Hospital
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- ot Yet Recruiting
- Sex
- Not specified
- Target Recruitment
- 0
Inclusion Criteria
ASA grade I and II.
No other associated cardiovascular/ respiratory disease
Exclusion Criteria
Patient with known hypersensitivity to local anaesthetics.
Patients with opioids addiction.
Patient with any local infection at site.
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Duration of analgesia <br/ ><br> <br/ ><br>Time of First onset of pain and time of first request for analgesia <br/ ><br>Timepoint: In Postoperative ward, the patient will be assessed for the presence and severity of pain at rest and on movement by VAS, nausea, vomiting and any other side effects at intervals of 2, 4, 6, 8, 12, 24 hours. <br/ ><br>
- Secondary Outcome Measures
Name Time Method Hemodynamic and Respiratory stability <br/ ><br> <br/ ><br>Any side effects or complications of study drugs and blocks <br/ ><br>Timepoint: The vitals heart rate NIBP & SPO2 will be recording for 30 minutes and at 2 4 6 8 12 24 hours postoperatively