Effect of a local pain relief patch after cesarean section on pain management.
Not Applicable
Not yet recruiting
- Conditions
- Health Condition 1: O82- Encounter for cesarean delivery without indication
- Registration Number
- CTRI/2023/04/051718
- Lead Sponsor
- MS Ramaiah Medical college
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Not Yet Recruiting
- Sex
- Not specified
- Target Recruitment
- 0
Inclusion Criteria
Patients between 18years to 50 years of age undergoing elective cesarean section under spinal anesthesia.
Exclusion Criteria
Patients who have undergone 3 or more prior Cesarean sections.
Patients allergic to drug Lidocaine.
Patients with recognizable contraindication to neuraxial block.
Need of tracheal intubation or use of supraglottic device during Cesarean section.
Patients with pregnancy induced hypertension.
Any incision other than the pfannensteil incison of cesarean section.
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method The potential post operative analgesic effect of 5% lidocaine patch in women undergoing Cesarean section under spinal anesthesia.Timepoint: The potential post operative analgesic effect of 5% lidocaine patch in women undergoing Cesarean section after 12hrs and 24hrs of surgery.
- Secondary Outcome Measures
Name Time Method Cumulative analgesic consumption in the first 24 hours post surgery.Timepoint: Pain assessed at intervals of 1 hour , 6 hours, 12 hours and 24 hours after surgery.