Evaluation of post-cesarean pain After Intraperitoneal Lidocaine Instillation versus intravenous lidocaine

Not Applicable

• Conditions: Surgery; analgesia and prevention of pain; Anaesthesia

• Registration Number: PACTR201506001145361
• Lead Sponsor: benha university hospital

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Results First Posted: 1900-01-01
• Study Start: 2015-05-16
• Last Update Posted: 29 May 2023

Recruitment & Eligibility

• Status: Complete
• Sex: Female
• Target Recruitment: 110

Inclusion Criteria

1-Singleton pregnancy,
2-more than or equal completed 37 gestational weeks,
3-indicated to undergo elective cesarean delivery for various indications e.g., primigravida with breech presentation, macrosomia, intrauterine growth restriction and contracted pelvis,
4-willing to participate in the study.

Exclusion Criteria

1-extreme of age (below 18 ¿ above 40 year),
2-uncooperative patients,
3-previous abdominal scars, including previous cesarean or myomectomy, multiple gestation,
4-BMI >35 kg/m², chorioamnionitis, hypersensitivity or contraindications to lidocaine,
5-bronchial asthma,
6-bleeding diathesis,
7-pregnancy induced-hypertension,
8-liver or kidney diseases,
9-diabetes mellitus,
9-patients with psychological disturbance, 10-any form of chronic pain before or during pregnancy

Study & Design

• Study Type: Interventional
• Study Design: Not specified