post-operative pain after rhinoplasty. Acute pain, not elsewhere classified
Conditions
Interventions
Intervention 1: The intervention group will receive 300 mg of gabapentin capsules one hour before the start of the study. Intervention 2: The control group will receive 300 mg of placebo capsules an
Sponsors
Kermanshah University of Medical Sciences
Eligibility
Sex/Gender
All
Inclusion criteria
Inclusion criteria: No history of diabetes, kidney and liver disease No history of drug abuse
Exclusion criteria
Exclusion criteria: Patients who has used Painkiller daily or within 24 hours before surgery Patients who use antidepressants, anti-epilepsy or antihypertensive drugs
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Intensity of pain. Timepoint: Beginning of study, 2, 4, 6, 12 and 24 hours after surgery. Method of measurement: Visual Analogue Scale(VAS). | — |
Countries
Iran (Islamic Republic of)
Contacts
Public ContactMasomeh Foladvand
Kermanshah University of Medical Sciences
Outcome results
None listed