Clinical trial the effect of intravenous ondansetron and sub-hypnotic propofol dose on pruritus after intrathecal opioid in patient with elective cesarean surgery

Phase 2

• Conditions: Condition 1: opioid induced pruritus. Condition 2: nausea and vomiting.; Pruritus, unspecified; Vomiting of pregnancy, unspecified

• Registration Number: IRCT2017041527677N7
• Lead Sponsor: Vice Chancellor for research of Urmia University of Medical Sciences

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Results First Posted: 1900-01-01
• Last Update Posted: 22 February 2018

Recruitment & Eligibility

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

Inclusion Criteria

20 to 40 years old; patient with class I and II America society of Anesthesiologists; cesarean surgery with spinal anesthesia
Exclusion criteria: any complaints of pruritus before surgery; start pruritus before closing cord; allergy to medications; preeclampsia; eclampsia; people who had used anti-nausea drug in the past 24 hours.

Exclusion Criteria

Not provided

Study & Design

• Study Type: interventional
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
Pruritus. Timepoint: During the surgery and recovery. Method of measurement: visual analog scale.

Secondary Outcome Measures

Name	Time	Method
ausea and vomiting. Timepoint: During the surgery and recovery. Method of measurement: Has- does not have.