pain after surgery. Pain, not elsewhere classified
Conditions
Interventions
Intervention 1: Intervention group: We treat patients 150 miligeram pregabalin 2 hours before surgery in intervention group.?. Intervention 2: Intervention group: We treat patients 1 gram Apotel in 2
Treatment - Drugs
Intervention group: We treat patients 150 miligeram pregabalin 2 hours before surgery in intervention group.?
Intervention group: We treat patients 1 gram Apotel in 200 milliliter 20 minute before surgery in intervention group.?
Control group: We treat patients one capsule placebo before surgery in intervention group.?
Sponsors
Arak University of Medical Sciences
Eligibility
Sex/Gender
All
Age
17 Years to 65 Years
Inclusion criteria
Inclusion criteria: candidate orthopedic surgery ?lower limb 17 to 65 years both of two gender
Exclusion criteria
Exclusion criteria: Coagulation disorders Unwillingness to participate in the study Severe hemodynamic instability Hepatic, renal and cardiac disease Sensitivity to Pregabalin and Apotel
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Pain. Timepoint: We record pain in recovery, 2 and 12 and 24 hours after surgery. Method of measurement: Visual Analog Sacle.;Consumption of opioids. Timepoint: We record consumption of opioids in 24 hours in milligram. Method of measurement: milligram.;Sedation. Timepoint: We record ramsy sedation score in 24 hours after surgery.?. Method of measurement: ramsy sedation score. | — |
Countries
Iran (Islamic Republic of)
Contacts
Public ContactDr Alireza Kamali
Arak University of Medical Sciences
Outcome results
None listed