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Effect of Metoclopramide infusion on postoperative analgesia in cesarean sectio

Phase 3
Conditions
caesarean surgery.
Delivery by caesarean section, unspecified
Registration Number
IRCT2017031232676N2
Lead Sponsor
Vice Chancellor for Research of Mazandaran University of Medical Sciences
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Complete
Sex
Female
Target Recruitment
100
Inclusion Criteria

Elective cesarean surgery; patients aged 20-35 years; American Society of Anesthesiologists (ASA) class I and II.
Exclusion criteria: indisposition; emergency section; prolonged surgery; smoking and narcotic user; psychiatric disorders.

Exclusion Criteria

Not provided

Study & Design

Study Type
interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Pain. Timepoint: During 24 hours after the surgry, at time 2, 4, 6, 12, 18, 24. Method of measurement: visual analog scale from 0 (without pain) to 10 (extremely pain).
Secondary Outcome Measures
NameTimeMethod
Ponv. Timepoint: During 24 hour after the surgery. Method of measurement: Visual Analog Scale.
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