Clinical Trials Directory

Trials / Completed

CompletedNCT06142591

Oxycodone (10, 20 mg) in a Postoperative Dressing

Oxycodone (10, 20 mg) in a Postoperative Dressing in Patients After Surgical Debridement of Burn Wounds. A Prospective, Double-blinded, Randomized, Controlled Trial.

Status
Completed
Phase
Phase 4
Study type
Interventional
Enrollment
20 (actual)
Sponsor
Poznan University of Medical Sciences · Academic / Other
Sex
All
Age
18 Years – 100 Years
Healthy volunteers
Not accepted

Summary

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

Detailed 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.

Conditions

Interventions

TypeNameDescription
DRUGOxycodone 10mg10mg of oxycodone was added to Octenisept in the wound dressing.
DRUGOxycodone 20mg20mg of oxycodone was added to Octenisept in the wound dressing.

Timeline

Start date
2016-01-01
Primary completion
2018-02-28
Completion
2022-03-03
First posted
2023-11-21
Last updated
2023-11-21

Source: ClinicalTrials.gov record NCT06142591. Inclusion in this directory is not an endorsement.