A comparison of pain relief from three different drug regimes for women undergoing cesarean sectio

Phase 1

Recruiting

• Conditions: post-operative pain inPatients undergoing cesarean section; post-operative pain in; Patients undergoing cesarean section; Anaesthesiology - Pain management; Reproductive Health and Childbirth - Childbirth and postnatal care; Surgery - Other surgery

• Registration Number: ACTRN12611000729921
• Lead Sponsor: Qazvin Medical Science University

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Study Start: 2011-07-13
• Last Update Posted: 13 January 2020

Recruitment & Eligibility

• Status: Recruiting
• Sex: Female
• Target Recruitment: 90

Inclusion Criteria

patients with American Society of Anesthesiologists(ASA) physical status I and II, undergoing elective cesarean section

Exclusion Criteria

significant coexisting disease such as hepato-renal and cardiovascular disease, any contraindication to regional anesthesia such as local infection or bleeding disorders, allergy to ketamine or midazolam , long-term opioid use or a history of chronic pain.

Study & Design

• Study Type: Interventional
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
Time to first requirement of analgesic supplement(analgesic administration was initiated by patient request(verbal rating scale[ VRS]>4)[Time to first requirement of analgesic supplement from the time of injection intrathecal anesthetic solution]