Status:
COMPLETED
Tramadol iv. : Influence of Dose and Dose Intervals on Therapeutic Accuracy and Side Effects When Used for Postoperative Pain Relief in Ambulatory Surgery
Lead Sponsor:
University Hospital, Ghent
Conditions:
Ambulatory Surgery
Eligibility:
All Genders
18-70 years
Phase:
PHASE2
Brief Summary
The aim of this study is to compare the administration of 1 unit dose of 100 mg tramadol intravenously versus multiple smaller dosages of tramadol during the first 6 hours post-operatively and to inve...
Eligibility Criteria
Inclusion
- ASA I and II female or male patients
- 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 :
September 1 2006
Trial Type :
INTERVENTIONAL
Allocation :
ESTIMATED
End Date :
April 1 2009
Estimated Enrollment :
200 Patients enrolled
Trial Details
Trial ID
NCT00333346
Start Date
September 1 2006
End Date
April 1 2009
Last Update
August 31 2010
Active Locations (1)
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1
University Hospital Ghent
Ghent, Belgium, 9000