Effect of metoclopramide on postoperative nausea and vomiting
Not Applicable
- Conditions
- postopertive pain.
- Registration Number
- IRCT201011054819N1
- Lead Sponsor
- Isfahan University of Medical Sciences
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Complete
- Sex
- All
- Target Recruitment
- 86
Inclusion Criteria
18-65 years old male and female patients with ASA1-2, no hypersensitivity to Ketamine or Metochlopramide who are candidates for elective laparotomy surgery under general anesthesia
Exclusion criteria: severe bleeding during anesthesia and need to blood transfusion during surgery
Exclusion Criteria
Not provided
Study & Design
- Study Type
- interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Postoperative pain. Timepoint: At 30th and 60th minutes at the recovery room and 2, 4, 6, and 24 hours postoperatively. Method of measurement: visual anlogue scale (VAS).
- Secondary Outcome Measures
Name Time Method Recovery stay time. Timepoint: end of recovery stay. Method of measurement: in minutes.;Amounts of opoid consumption. Timepoint: At the recovery room and over 24 hours postoperatively. Method of measurement: in mg.;Amounts of ondansetron consumption. Timepoint: Over 24 hours postoperatively. Method of measurement: in mg.;Postoperative nausea and vomiting. Timepoint: At the recovery room and 6, 12, and 24 hours postoperatively. Method of measurement: observation and VAS.;Irritability. Timepoint: at recovery room. Method of measurement: observation.;Psychologic problems. Timepoint: at recovery. Method of measurement: observation.