The effect of intraperitoneal instillation of Lidocaine on the postoperative pain after cesarean delivery

Status

Active, not recruiting

Phases

Phase 3

Study type

Interventional

Source

IRCT

Registry ID

IRCT20190227042862N1

Enrollment

200

Registered

2019-05-23

Start date

2018-11-22

Completion date

Unknown

Last updated

2019-08-26

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

Conditions

Cesarean section. Single delivery by caesarean section

Interventions

Intervention 1: Intervention group: After delivery of the neonate and placenta, and the surgeon satisfaction with hemostasis, a sterile 20-mL syringe containing 2% lidocaine with epinephrine 1:200,000

Eligibility

Sex/Gender

Female

Age

18 Years to 45 Years

Inclusion criteria

Inclusion criteria: All pregnant women with singleton pregnancy between 18 to 45 years body mass index (BMI) less than 40 one previous cesarean section with pfannenstiel incision candidate for elective cesarean section with spinal anesthesia

Exclusion criteria

Exclusion criteria: history of other abdominal surgery history of chronic pain history of cardiac arrhythmia Sensitivity to the drugs which are used in the intervention group

Design outcomes

Primary

Measure	Time frame
Post-operative pain. Timepoint: 6, 12 and 24 hours after cesarean section. Method of measurement: Visual Analogue Scale.	—

Countries

Iran (Islamic Republic of)

Contacts

Public ContactRazieh Hadi

Mashhad University of Medical Sciences

hadir931@mums.ac.ir+98 51 3278 2261

Outcome results

None listed

Source: IRCT (via WHO ICTRP) · Data processed: Feb 4, 2026