Post-operative pain control. Acute pain
Conditions
Interventions
Intervention 1: Patients in the case group will receive 15 mg/kg bodyweight apotel (interavenous acetaminophen) half an hour before the start of surgery. Surgery will be performed as usual and then, b
Treatment - Drugs
Patients in the case group will receive 15 mg/kg bodyweight apotel (interavenous acetaminophen) half an hour before the start of surgery. Surgery will be performed as usual and then, based on the pain
In the patients of control group, surgery is performed as usual, and after then, based on the pain intensity, an analgesic drug (pethidine) will be given to the patients and they will not receive anot
Sponsors
Research deputy Birjand University of Medical Science
Eligibility
Sex/Gender
All
Age
20 Years to 50 Years
Inclusion criteria
Inclusion criteria: Inclusion criteria: Inguinal hernia; surgical candidate for ASA classes 1 and 2; age 20-50 years Exclusion criteria: drug addiction; history of chronic diseases, diabetes, heart failure, hypertension etc; neuropsychological diseases
Exclusion criteria
Exclusion criteria:
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Mean of opioid consumption. Timepoint: 1, 2, 4, 8, 12 and 24 hours after surgery. Method of measurement: mg/kg. | — |
Secondary
| Measure | Time frame |
|---|---|
| Pain. Timepoint: 1, 2, 4, 8, 12 and 24 hours after surgery. Method of measurement: VAS. | — |
Countries
Iran (Islamic Republic of)
Contacts
Public ContactDr Seyed Amirkazem Vejdan
Birjand University of Medical Sciences
Outcome results
None listed