Trials / Completed

CompletedNCT00333346

Tramadol iv. : Influence of Dose and Dose Intervals on Therapeutic Accuracy and Side Effects When Used for Postoperative Pain Relief in Ambulatory Surgery

Status: Completed
Phase: Phase 2
Study type: Interventional
Enrollment: 200 (estimated)

Sponsor: University Hospital, Ghent · Academic / Other
Sex: All
Age: 18 Years – 70 Years
Healthy volunteers: Not accepted

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 investigate the time course and accuracy of pain relief versus the onset and duration of side-effects.

Conditions

Ambulatory Surgery

Interventions

Type	Name	Description
DRUG	Administration of tramadol intravenously

Timeline

Start date: 2006-09-01
Primary completion: 2009-04-01
Completion: 2009-04-01
First posted: 2006-06-05
Last updated: 2010-08-31

Locations

1 site across 1 country: Belgium

Source: ClinicalTrials.gov record NCT00333346. Inclusion in this directory is not an endorsement.