Patients candidate for orthopedic Plating’s Surgery.
Conditions
Interventions
Intervention 1: Intervention group 1: Ketorolac group. Intervention 2: Intervention group 2: Methadone group.
Sponsors
Zahedan University of Medical Sciences
Eligibility
Sex/Gender
All
Age
15 Years to 55 Years
Inclusion criteria
Inclusion criteria: AGE 15-55years No underlying disease ASA CLASS I&II General anesthesia Plating’s Orthopedic Surgery’s cases
Exclusion criteria
Exclusion criteria: Drug addict Preoperative hemodynamic unstability Blood loss that needs Transfusion of Packed Red Cells Take a drug that effects on hemodynamic Informed consent not signed
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Reduced pain score in patients. Timepoint: Pain will be evaluated at the beginning of study and 0.5, 1 and 6 hours after intervention. Method of measurement: Visual acuity scale.;Heart rate. Timepoint: Pain will be evaluated at the beginning of study and 0.5, 1 and 6 hours after intervention. Method of measurement: Heart contraction by ECG monitor.;Blood pressure. Timepoint: Pain will be evaluated at the beginning of study and 0.5, 1 and 6 hours after intervention. Method of measurement: Blood pressure on monitor.;Nausea & Vomit. Timepoint: Pain will be evaluated at the beginning of study and 0.5, 1 and 6 hours after intervention. Method of measurement: Asking Patient.;Asking for morphine. Timepoint: Pain will be evaluated at the beginning of study and 0.5, 1 and 6 hours after intervention. Method of measurement: Number of doses patient asking for. | — |
Countries
Iran (Islamic Republic of)
Contacts
Public ContactSomayye heidarpour
Zahedan University of Medical Sciences
Outcome results
None listed