pain.
Conditions
Interventions
Intervention 1: Intervention group: "Elective subjects who were randomly assigned to receive alprazolam half a milligram a day before surgery". Intervention 2: Control group: A number of elective abdo
Sponsors
Islamic Azad University
Eligibility
Sex/Gender
All
Age
20 Years to 60 Years
Inclusion criteria
Inclusion criteria: Elective abdominal surgery Consent letter for study A.S.A class I and II Age between 20 to 60 No allergy to Alprazolam No history of opium addiction
Exclusion criteria
Exclusion criteria: Operation time more than 3 hours Post operative delirium Complicated surgery
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Intensity of pain. Timepoint: in recovery, 4 and 24 hours after surgery. Method of measurement: Visual Analogue Scale ruler. | — |
Secondary
| Measure | Time frame |
|---|---|
| Postoperative pain. Timepoint: in recovery, 4 and 24 hours after surgery. Method of measurement: Visual Analogue Scale ruler. | — |
Countries
Iran (Islamic Republic of)
Contacts
Public ContactFarshid Gholami
Islamic Azad University
Outcome results
None listed