comparative study to identify effect levobupivacaine vs bupivacaine in spinal anesthesia for below umbilical surgeries
- Conditions
- Health Condition 1: O- Medical and SurgicalHealth Condition 2: O- Medical and Surgical
- Registration Number
- CTRI/2023/02/049446
- Lead Sponsor
- sri manakula vinayagar medical college and hospital
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- ot Yet Recruiting
- Sex
- Not specified
- Target Recruitment
- 0
1.Patients scheduled to undergo elective infra umbilical surgeries under spinal anesthesia for next one year from the date of clearance from Ethical committee.
2. Patients of ASA physical status 1 & 2.
3. Patients of either sex.
4. Age >18 years or < 60 years.
5. Patients with height more than 150 cm
1. Body Mass Index >30.
2. Patients with local site infection, allergy to the drugs that are to be tested
or any othercontraindications for spinal anesthesia.
3. Patients who cannot lie down/ non-co-operative/ psychiatric illness.
4. Alcoholics.
5. Pregnant / Lactating women.
6. Patient having failed spinal, transformed into general anesthesia will be excluded from
study.
7. Patients refusal for participation in the study.
8. Patients with height less than 150 cm.
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method To compare the sub-arachnoid block characteristics between 0.5% hyperbaric Levobupivacaine and 0.5% hyperbaric bupivacaine in below umbilical surgeries.Timepoint: to assess the sensory blockade every 2 mins till 20mins <br/ ><br>to assess the motor blockade every 5mins till maximum level achieved
- Secondary Outcome Measures
Name Time Method to assess difference in hemodynamic parameter between both the groups <br/ ><br>to assess the adverse reaction between two groupsTimepoint: 10mins before spinal then at 5 mins every 10 mins for the first half an hour and at 1 hr 2 hrs