Burns Clinical Trial - Oxycodone (10, 20 mg) in a Postoperative Dressing

Status Completed

Clinical Trial Summary

The study mainly focuses on pain management using 10- or 20mg oxycodone burn wound dressing at Poznan University of Medical Sciences.

Clinical Trial Description

Subjects were randomly assigned to one of the two treatment groups, A and B. Patients scheduled for burn surgery will sign written consent pre-operatively about procedural pain management. Group A received 10mg of oxycodone in wound dressing, while those in Group B received 20mg of oxycodone in wound dressing. ;

Study Design

Related Conditions & MeSH terms

Burns

Clinical Trial Details

NCT number	NCT06142591
Study type	Interventional
Source	Poznan University of Medical Sciences
Contact
Status	Completed
Phase	Phase 4
Start date	January 1, 2016
Completion date	March 3, 2022

View Details

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