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
| Type | Name | Description |
|---|---|---|
| DRUG | Oxycodone 10mg | 10mg of oxycodone was added to Octenisept in the wound dressing. |
| DRUG | Oxycodone 20mg | 20mg 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.