Condition 1: Postoperative pain. Condition 2: Postoperative nausea.
Conditions
Interventions
Intervention 1: Intervention group 1: Intravenous injection of 0.15mg/kg metoclopramide in 5 cc normal saline and subcutaneous injection of 5cc normal saline. Intervention 2: Intervention group 2: S
Sponsors
Esfahan University of Medical Sciences
Eligibility
Sex/Gender
All
Age
18 Years to 65 Years
Inclusion criteria
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
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
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| 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
| Measure | Time frame |
|---|---|
| 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. | — |
Countries
Iran (Islamic Republic of)
Contacts
Public ContactHamid Haji Gholam Saryazdi
Esfahan University of Medical Sciences
Outcome results
None listed