Subcutaneous wound infiltration with tramadol for post cesarean section pain relief: a randomized controlled trial

Not Applicable

• Conditions: Pregnancy and Childbirth; Surgery; Postoperative pain

• Registration Number: PACTR201711002756172
• Lead Sponsor: Air-Force Specialized Hospital

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Results First Posted: 1900-01-01
• Study Start: 2017-11-11
• Last Update Posted: 29 May 2023

Recruitment & Eligibility

• Status: Complete
• Sex: Female
• Target Recruitment: 99

Inclusion Criteria

All women undergoing elective cesarean section

Exclusion Criteria

Major medical disorders
Bleeding tendency
Allergy to medication
Drug addiction

Study & Design

• Study Type: Interventional
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
Post-operative pain

Secondary Outcome Measures

Name	Time	Method
need for post-operative analgesia