Evaluation of the effect of oral Oxycodone and Saphenous nerve block in knee replacement surgery
Not Applicable
- Conditions
- Regional Anesthesia and Pain Management.Acute pain
- Registration Number
- IRCT20170826035905N3
- Lead Sponsor
- Baqiyatallah University of Medical Sciences/Trauma Research Center
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Complete
- Sex
- All
- Target Recruitment
- 80
Inclusion Criteria
Age between 15 and 75 years
Candidates for knee replacement surgery
Classification for American Society of Anesthesiology (ASA) I, II (patients with normal or mild and controlled underlying disease).
Exclusion Criteria
Previous knee joint surgery
Bilateral surgery
Kidney or liver function disorders,
History of allergic sensitization to non-steroidal anti-inflammatory drugs
History of addiction
History of chronic drug use for pain control
History of severe cardiovascular or respiratory disease
History of neurological disease with lower limb involvement
History of gastrointestinal ulcer
Failure of block
Study & Design
- Study Type
- interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Pain. Timepoint: 2,6,12,24 hours after surgery. Method of measurement: Visual Analog Scale.
- Secondary Outcome Measures
Name Time Method ausea. Timepoint: 2,6,12,24 hours after surgery. Method of measurement: Rating variable :Mild(0-1) Moderate(2-3) Severe(more than 3).;Sedation. Timepoint: 2,6,12,24 hours after surgery. Method of measurement: Rating variable :Mild(0-1) Moderate(2-3) Severe(more than 3).