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NCT00369811 Clinical Trial

Oxycodone vs Fentanyl for Pain Treatment After Laparoscopic Cholecystectomy

Pain Clinical Trial

Official title:
Comparative Study of Oxycodone and Fentanyl Given Intravenously in the Treatment of Early Postoperative Pain After Laparoscopic Cholecystectomy

Clinical Trial Details — Status: Completed

Administrative data
NCT number NCT00369811
Other study ID # OXFEN2006
Secondary ID
Status Completed
Phase Phase 4
First received August 28, 2006
Last updated November 16, 2007
Start date August 2006
Est. completion date September 2007

Study information
Verified date November 2007
Source Danish Pain Research Center
Contact n/a
Is FDA regulated No
Health authority Denmark: Danish Medicines Agency
Study type Interventional

Clinical Trial Summary

To evaluate the analgesic efficacy of oxycodone and fentanyl in the treatment of postoperative pain after laparoscopic cholecystectomy.

Recruitment information / eligibility
Status Completed
Enrollment 80
Est. completion date September 2007
Est. primary completion date
Accepts healthy volunteers No
Gender Female
Age group 18 Years and older
Eligibility Inclusion Criteria:

- Planned outpatient laparoscopic cholecystectomy

- >18 years

Exclusion Criteria:

- Intolerance to study drugs

- Treatment with MAO inhibitors

Study Design

Allocation: Randomized, Endpoint Classification: Efficacy Study, Intervention Model: Parallel Assignment, Masking: Double-Blind, Primary Purpose: Treatment

Related Conditions & MeSH terms

Intervention

Drug:
• Oxycodone, fentanyl

Locations
Country Name City State
Denmark Department of Anesthesiology, Aarhus University Hospital Aarhus

Sponsors (1)
Lead Sponsor Collaborator
Danish Pain Research Center

Country where clinical trial is conducted

Denmark, 

Outcome
Type Measure Description Time frame Safety issue
Primary Pain intensity
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