Patients with upper limb fractures..
Conditions
Interventions
Intervention 1: Intervention group: the pain pump will contain 2 grams of Apotel and 8 milligrams of Ondansetron, which will be diluted with 100 cc normal saline 0.9 % and will be delivered at the rat
Treatment - Drugs
Control group:the pain pump will contain 2 grams of Apotel, which will be diluted with 100 cc normal saline 0.9 % and will be delivered at the rate of 4 cc / hr.
Intervention group: the pain pump will contain 2 grams of Apotel and 8 milligrams of Ondansetron, which will be diluted with 100 cc normal saline 0.9 % and will be delivered at the rate of 4 cc / hr.
Sponsors
Vice chancellor for research, Golestan University of Medical Sciences
Eligibility
Sex/Gender
All
Age
15 Years to 90 Years
Inclusion criteria
Inclusion criteria: Inclusion criteria: ASA Class 1; Upper limb fracture; Patients who undergo anesthesia with propofol as an anesthetic inducer; Satisfied to participate in the study; being at the age of 15 and older. Exclusion criteria: ASA grade 3 and 4; uncontrolled diabetes; history of ischemic heart disease (IHD); history of stroke; malignancy; psychiatric problems; Pregnancy; surgery duration greater than 120 minutes; history of substance abuse or drug abuse; Alcohol consumption; history of liver problems; history of Apotel (acetaminophen) sensitivity; history of nausea and vomiting after previous surgical procedure; Patients with long Q-T intervals.
Exclusion criteria
Exclusion criteria:
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Pain. Timepoint: 24 hours and 48 hours after recovery. Method of measurement: Visual Analogue Scale. | — |
Countries
Iran (Islamic Republic of)
Contacts
Public ContactDr Mohammadhosein Taziki
Golestan University of Medical Sciences
Outcome results
None listed