Study comparing the effects of 0.75% Ropivacaine heavy and 0.5% Bupivacaine heavy in intrathecal injections during elective procedures
Not Applicable
- Conditions
- Health Condition 1: O- Medical and Surgical
- Registration Number
- CTRI/2023/08/056690
- Lead Sponsor
- Others
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- ot Yet Recruiting
- Sex
- Not specified
- Target Recruitment
- 0
Inclusion Criteria
study will be done on eighty cases of either sex of ASA class-I or II between age group of 18-60 years weighing between 50-70kgs and height 160-170 cms scheduled for elective surgeries
Exclusion Criteria
Any h/o respiratory, cardiac, hepatic or renal disease, convulsions
Patients with h/o bleeding disorder
local infection at the site of injection
H/o allergy to local anesthetic agent
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Onset of sensory block <br/ ><br>Duration of sensory block <br/ ><br>onset of motor block <br/ ><br>duration of motor blockTimepoint: Baseline, 2 minutes, 4 minutes, 6 minutes, 8 minutes
- Secondary Outcome Measures
Name Time Method incidence of urinary retention, anaphylaxis, postoperative nausea and vomitingTimepoint: 06 hours, 12 hours, 24 hours