Pain. Other acute postprocedural pain
Conditions
Interventions
Intervention 1: Intervention group1 : The intervention will be one hour before the operation, receive a single dose of 300 mg Pregabalin orally and 100 cc of 0.9% normal saline by infusion 30 minutes
Sponsors
Bojnourd University of Medical Sciences
Eligibility
Sex/Gender
All
Age
20 Years to 60 Years
Inclusion criteria
Inclusion criteria: Age between 20 to 60 years ASA physical status I-II Do not have drug addiction Do not have allergic to Pregabalin and Paracetamol
Exclusion criteria
Exclusion criteria: If the patient have used paracetamol or pregabalin 48 hours before the operation. If the patient be suffering from neurological and psychological, heart, lung, kidney and liver disease. If the patient has any history of epilepsy.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Pain. Timepoint: Recovery, 12, 24 and 48 hours after surgery. Method of measurement: Visual Analog Score (VAS) Form of pain. | — |
Secondary
| Measure | Time frame |
|---|---|
| Pregabalin and Paracetamol Side Effects. Timepoint: Up to 48 hours after surgery. Method of measurement: Examination and observation of the patient. | — |
Countries
Iran (Islamic Republic of)
Contacts
Public ContactJavad Shahinfar
Bojnourd University of Medical Sciences
Outcome results
None listed