A clinical study to compare two drugs for postoperative pain control.
Phase 4
Completed
- Conditions
- Health Condition 1: null- patients for lower segment caesarean sectionHealth Condition 2: O00-O9A- Pregnancy, childbirth and the puerperium
- Registration Number
- CTRI/2018/03/012729
- Lead Sponsor
- Dayanand medical college and hospital
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Completed
- Sex
- Not specified
- Target Recruitment
- 40
Inclusion Criteria
•Undergoing LSCS performed by Pfannenstiel incision (under spinal anaesthesia)
•ASA grade I or II
•Not having any systemic disorders.
•Age group 20 - 35 years
Exclusion Criteria
•Patients with history of allergy to local anaesthetics, opioids and/or drugs to be used.
•Patients with history of drug abuse.
•Patients with psychiatric disease.
•Morbidly obese patients.
•Patients unable to understand Visual Analogue Scale (VAS).
•Failed spinal anaesthesia and conversion to general anaesthesia.
•Duration of surgery greater than 2 hours.
•Uncooperative and unwilling patients
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method DURATION OF PAIN FREE PERIOD <br/ ><br>Timepoint: DURATION OF PAIN FREE PERIOD <br/ ><br>-24 HOURS
- Secondary Outcome Measures
Name Time Method RESCUE ANALGESIC CONSUMPTION AND ANY ADVERSE EFFECTSTimepoint: 24 HOURS