To compare post operative pain relief using drugs dexmedetomidine and fentanyl added to bupivacaine in lower abdominal surgery.
Phase 3
- Conditions
- Health Condition 1: - Health Condition 2: O- Medical and Surgical
- Registration Number
- CTRI/2024/02/062910
- Lead Sponsor
- Konjengbam Reshmi Devi
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- ot Yet Recruiting
- Sex
- Not specified
- Target Recruitment
- 0
Inclusion Criteria
1. American Society of Anaesthesiologists (ASA) physical status I and II.
2. 18- 65 years of age.
3. Either sex
Exclusion Criteria
1. History of allergy to study drugs
2. Bleeding disorder
3. Local site infection
4. Cardiac,respiratory and kidney disorder,neurological deficit
5.Spinal deformity
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method To compare the duration of postoperative Analgesia (demand of first rescue analgesia)in first 24 hoursTimepoint: Outcome will be assessed at 24 hours post-op
- Secondary Outcome Measures
Name Time Method 1. Hemodynamic parameters- Heart rate (HR), systolic blood pressure (SBP), diastolic blood pressure (DBP), mean arterial pressure (MAP), oxygen saturation (spo2) <br/ ><br>2. Adverse effects.Timepoint: Outcome will be assessed at baseline <br/ ><br>2min intra-op <br/ ><br>4min intra-op <br/ ><br>6min intra-op <br/ ><br>8min intra-op <br/ ><br>10min intra-op <br/ ><br>then every 5 min after 10 min intraoperatively & for 24 hour period post op to see any adverse effect