Efficacy of Intraperitoneal Lidocaine in Cesarean Sections to Control Post-Operative Pain

Status

Recruiting

Phases

Unknown

Study type

Interventional

Source

PACTR

Registry ID

PACTR202411462637073

Enrollment

100

Registered

2024-11-26

Start date

2024-09-01

Completion date

Unknown

Last updated

2026-09-14

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

Conditions

Pregnancy and Childbirth

Interventions

Group A

Group B

Eligibility

Sex/Gender

Female

Inclusion criteria

Inclusion criteria: Age 20-45 years Undergoing elective CS Under Spinal anesthesia BMI <40kg/m2

Exclusion criteria

Exclusion criteria: • History of noted allergy to drug used in study Medical disorders Any other surgical procedure other than the CS (like salpingectomy or oophorectomy) Substance abuse Intraoperative complications (such as bowel or bladder injuries)

Design outcomes

Primary

Measure	Time frame
VAS pain score	—

Secondary

Measure	Time frame
Consumption of opioids;Intestinal motility (onset of passing of flatus or stool);Onset of ambulation;Hospital stay	—

Countries

Egypt

Contacts

Public ContactHatem Elsayed

Lecturer of obstetrics and gynecology in Ain Shams University Maternity Hospital

hatemelsayed2011@yahoo.com00201009525878

Outcome results

None listed

Source: PACTR (via WHO ICTRP) · Data processed: Sep 19, 2026