Comparison of two local anaesthetics in spinal anaesthesia
Not yet recruiting
- Conditions
- Medical and Surgical,
- Registration Number
- CTRI/2022/04/041908
- Lead Sponsor
- Sree Balaji Medical College and Hospital
- Brief Summary
0.75% ropivacaine has equal potency to 0.5% bupivacaine and Ropivacaine has been proven to be safer than Bupivacaine. However, Bupivacaine is still commonly used in our country and readily-available 0.75% hyperbaric ropivacaine has not been studied so far in the Indian population. Hence, we are planning to conduct this study.
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Not Yet Recruiting
- Sex
- All
- Target Recruitment
- 60
Inclusion Criteria
ASA 1&2 Undergoing infra umbilical surgery under subarachnoid block Consenting to participate in the study.
Exclusion Criteria
Patient refusal Allergy to local anaesthetics Local infection at the site of block Bleeding disorder Pre operative hypotension pregnancy.
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method onset and duration of sensory block The onset of sensory block at T10 will be monitored from positioning the patient after spinal anaesthesia at every 30 seconds and thereafter at every 3 minutes for the 1st 15 minutes and at every 30 minutes till it recedes to S2
- Secondary Outcome Measures
Name Time Method onset and duration of motor block motor block will be monitored from 0 minute at 30 seconds interval till grade 3 block according to modified Bromage scale is achieved and at 30 minutes interval till complete regression of motor block hemodynamic disturbance and complications. vital parameters will be monitored from 0 minute at 3 minute interval till 1st 15 minutes, at 10 minutes interval during the surgery and at 30 minutes interval till complete recovery. fall in MAP or SBP more than 30% or heart rate below 50/min requiring pharmacological treatment will be noted and patient followed up for 24 hours to note other complications such as nausea vomiting, rashes, urinary retention if any
Trial Locations
- Locations (1)
Sree Balaji Medical College and Hospital
🇮🇳Kancheepuram, TAMIL NADU, India
Sree Balaji Medical College and Hospital🇮🇳Kancheepuram, TAMIL NADU, IndiaDr Gayathri RameshPrincipal investigator9004645828docgayu@gmail.com