A study to compare the duration of pain relief with clonidine and morphine added to local anaesthetic drug Bupivacaine in spinal anaesthesia for patients undergoing vaginal hysterectomy.
Not Applicable
- Conditions
- Health Condition 1: O- Medical and Surgical
- Registration Number
- CTRI/2024/07/070200
- Lead Sponsor
- Rajesh Ravi
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- ot Yet Recruiting
- Sex
- Not specified
- Target Recruitment
- 0
Inclusion Criteria
undergoing Vaginal hysterectomy under spinal anesthesia
Exclusion Criteria
Patients who have contraindications for regional anaesthesia will be excluded from the study
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method To compare the duration of postoperative analgesic effect of intrathecal clonidine and morphine when used as adjuvants to hyperbaric bupivacaine in spinal anaesthesiaTimepoint: 24 hours
- Secondary Outcome Measures
Name Time Method 1. To compare postoperative pain scores in both groups. <br/ ><br> <br/ ><br>2. To compare side effects like sedation, bradycardia, hypotension, urinary retention, nausea, vomiting, Itching, dry mouth and post operative shivering. <br/ ><br> <br/ ><br>3. Time to regression of motor or sensory block <br/ ><br> <br/ ><br>4. Time to first oral intake <br/ ><br> <br/ ><br>5. Patient satisfaction scores <br/ ><br>Timepoint: 24 hours