The effect of metoclopramide on postoperative pain and nausea
Phase 3
- Conditions
- Condition 1: Postoperative pain. Condition 2: Postoperative nausea.
- Registration Number
- IRCT20190825044609N1
- Lead Sponsor
- Esfahan University of Medical Sciences
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Complete
- Sex
- All
- Target Recruitment
- 75
Inclusion Criteria
Patients aged 18-65 year referred to Al-Zahra hospital during the year 1396-1397 for elective lower abdominal surgery and classified as ASA physical status 1 & 2 were included
Exclusion Criteria
Pregnancy
Addiction to cigarette, opioid and alcohol
Weight over 100 kg
Allergy to metoclopramide
Chronic pain that lasts more than 6 months
Anxiety before surgery
Taking any analgesic 24 hours before surgery
Study & Design
- Study Type
- interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Intensity of postoperative pain. Timepoint: In extubation time, 15 minutes, 30 minutes, 60 minutes, 2 hours, 4 hours, 8 hours, 16 hours, 24 hours after surgery. Method of measurement: Questionnaire according to Visual Analogue Scale.;Intensity of postoperative nausea. Timepoint: In extubation time, 15 minutes, 30 minutes, 60 minutes, 2 hours, 4 hours, 8 hours, 16 hours, 24 hours after surgery. Method of measurement: Questionnaire according to Visual Analogue Scale.
- Secondary Outcome Measures
Name Time Method Blood pressure. Timepoint: In extubation time, 15 minutes, 30 minutes, 60 minutes, 2 hours, 4 hours, 8 hours, 16 hours, 24 hours after surgery. Method of measurement: manometer.;Heart rate. Timepoint: In extubation time, 15 minutes, 30 minutes, 60 minutes, 2 hours, 4 hours, 8 hours, 16 hours, 24 hours after surgery. Method of measurement: pulseoxymeter.