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| Sponsored by: |
Danish Pain Research Center |
| Information provided by: | Danish Pain Research Center |
| ClinicalTrials.gov Identifier: | NCT00369811 |
Purpose
To evaluate the analgesic efficacy of oxycodone and fentanyl in the treatment of postoperative pain after laparoscopic cholecystectomy.
| Condition | Intervention | Phase |
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Pain |
Drug: Oxycodone, fentanyl |
Phase IV |
| Drug Information available for: | Fentanyl Citrate Fentanyl Oxycodone Oxycodone hydrochloride |
| Study Type: | Interventional |
| Study Design: | Treatment, Randomized, Double-Blind, Active Control, Parallel Assignment, Efficacy Study |
| Official Title: | Comparative Study of Oxycodone and Fentanyl Given Intravenously in the Treatment of Early Postoperative Pain After Laparoscopic Cholecystectomy |
Eligibility
| Ages Eligible for Study: | 18 Years and older |
| Genders Eligible for Study: | Female |
| Accepts Healthy Volunteers: | No |
Inclusion Criteria:
Exclusion Criteria:
Contacts and Locations| Denmark | |||||
| Department of Anesthesiology, Aarhus University Hospital | |||||
| Aarhus, Denmark, 8000 | |||||
| Danish Pain Research Center |
| Principal Investigator: | Lone Nikolajsen, MD, PhD | Danish Pain Research Center, Aarhus University Hospital |
More Information
| Study ID Numbers: | OXFEN2006 |
| First Received: | August 28, 2006 |
| Last Updated: | November 16, 2007 |
| ClinicalTrials.gov Identifier: | NCT00369811 |
| Health Authority: | Denmark: Danish Medicines Agency |
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