Status:
COMPLETED
Comparison of Tramadol Orally Versus an Optimized Dose of Intravenous Tramadol for Postoperative Pain Relief in Ambulatory Surgery
Lead Sponsor:
University Hospital, Ghent
Conditions:
Pain
Eligibility:
All Genders
18-70 years
Phase:
PHASE4
Brief Summary
The purpose of this study is to compare the administration of 1 unit dose of 50 mg tramadol perorally given in 3 unit dosages versus tramadol IV given in 3 unit dosage of 35 mg during the first 6 hour...
Eligibility Criteria
Inclusion
- ASA I and II female or male patients undergoing wisdom teeth extraction
- Aged 18-70 years
- Scheduled for ambulatory surgery requiring postoperative pain medication
Exclusion
- Weight less than 70% or more than 130% of ideal body weight
- Neurological disorder
- Recent use of psycho-active medication, including alcohol
- Patients suffering from chronic pain receiving pre-operative pain medication including NSAID's
- Use of chronic anti-emetic medication
- Use of chronic corticoid therapy
Key Trial Info
Start Date :
March 1 2008
Trial Type :
INTERVENTIONAL
Allocation :
ACTUAL
End Date :
June 19 2009
Estimated Enrollment :
195 Patients enrolled
Trial Details
Trial ID
NCT00735748
Start Date
March 1 2008
End Date
June 19 2009
Last Update
January 9 2023
Active Locations (1)
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1
University Hospital Ghent
Ghent, Belgium, 9000