A comparative study to evaluate a better pain relief modality for postoperative patients
Not Applicable
- Conditions
- Health Condition 1: G541- Lumbosacral plexus disorders
- Registration Number
- CTRI/2021/11/038243
- Lead Sponsor
- Vydehi Institute of Medical Sciences and Research centre
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- ot Yet Recruiting
- Sex
- Not specified
- Target Recruitment
- 0
Inclusion Criteria
1.Patients with American Society of Anesthesiologists (ASA) I and II physical status.
2.Patients with age between 18 to 60 years of either sex
3.Elective lower abdominal surgeries.
4.Patients who have given written informed consent.
Exclusion Criteria
1.Patients with history of allergy to local anaesthetics.
2.Patients with mental illness.
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method â?¢Time of first rescue analgesic request <br/ ><br>â?¢Total analgesic drug requirement <br/ ><br>Timepoint: 30 minutes, 1 hour, 2 hours, 4 hours, 6 hours, 12 hours, 18 hours, 24 hours
- Secondary Outcome Measures
Name Time Method adverse eventsTimepoint: 24 hours