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

Tramsdol vs lidocaine vs placebo wound infiltration for post cesarean section pain relief: a randomized controlled trial

Status

Active, not recruiting

Phases

Unknown

Study type

Interventional

Source

PACTR

Registry ID

PACTR201711002756172

Enrollment

Registered

2017-11-11

Start date

2017-11-22

Completion date

Unknown

Last updated

2026-08-03

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Pregnancy and Childbirth Surgery Postoperative pain

Interventions

Saline

Lidocaine

Tramadol

Eligibility

Sex/Gender

Female

Inclusion criteria

Inclusion criteria: All women undergoing elective cesarean section

Exclusion criteria

Exclusion criteria: Major medical disorders Bleeding tendency Allergy to medication Drug addiction

Design outcomes

Primary

Measure	Time frame
Post-operative pain	—

Secondary

Measure	Time frame
need for post-operative analgesia	—

Countries

Egypt

Contacts

Public ContactAhmed Sherif

Ain-Shams Universaity

ahmedgyna@yahoo.com+201227960980

Outcome results

None listed

Source: PACTR (via WHO ICTRP) · Data processed: Aug 9, 2026