Comparison of spinal clonidine and buprenorphine for vaginal hysterectomy under spinal anaesthesia
Phase 4
Completed
- Conditions
- Health Condition 1: null- Female patients undergoing elective vaginal hysterectomy
- Registration Number
- CTRI/2018/05/013907
- Lead Sponsor
- Seth GS medical College and KEM hospital
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Completed
- Sex
- Not specified
- Target Recruitment
- 90
Inclusion Criteria
ASA 1-2
Age 35-70 years
Weight 40-70 kgs
Height more than 150cms
Patient undergoing vaginal hysterectomy under spinal anaesthesia
Exclusion Criteria
Patient refusal
on more than one antihypertensive agent
allergy to local anaesthetics
contraindication to spinal anaesthesia like raised intracranial pressure,coagulation disorder,infection at spinal site,spinal deformity,hypovolemia
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method time for onset of blockade,The upper and lower levels of sensory block were assessed after giving spinal block till regression of blockTimepoint: Degree of sensory and motor blockade was assessed every minute for first 10 minutes, every 2 minutes for next 10 minutes, every 15 minutes for next 1 hour and every 30 minutes there on. The assessment was continued till complete regression of sensory and motor block
- Secondary Outcome Measures
Name Time Method postoperative pain relief and rescue analgesics if needed,time needed for postoperative ambulation,time needed for 2 level regression of block,side effects if anyTimepoint: After closure of skin incision till patient was kept in recovery till 6 hours postoperatively