Trials / Unknown
UnknownNCT04422119
Standard Dressing Versus Moist Dressing in the Course of the Postoperative Wound in Patients With Knee Prosthesis
- Status
- Unknown
- Phase
- N/A
- Study type
- Interventional
- Enrollment
- 150 (estimated)
- Sponsor
- Germans Trias i Pujol Hospital · Academic / Other
- Sex
- All
- Age
- 18 Years
- Healthy volunteers
- Not accepted
Summary
The aim of the study is: to evaluate the efficacy of two post-operative dressings in the management of the surgical wounds in patients who received a knee prosthesis
Detailed description
This was a randomised, controlled, clinical trial on patients who received a primary knee prosthesis in 2018-2019. Treatment group was given a multi-layer foam dressing with Safetac. The control group received standard treatment with povidone-iodine and a gauze dressing with plaster. 50 patients was needed for sufficient power. Primary outcome measures were; the characteristics of the surgical wound, patient reported comfort and adaptability according to the physiotherapist. Secondary outcome measures were: the clinical status and quality of life level according to the Western Ontario and McMaster Universities Osteoarthritis Index (WOMAC). Statistical analysis was performed by using IBM SPSS version 25, with a statistical significance of 5%.
Conditions
Interventions
| Type | Name | Description |
|---|---|---|
| PROCEDURE | Multi-Foam dressing | Application of a multi-layer foam dressing with Safetac in surgical wound |
| PROCEDURE | Usual care | Care of surgical wound with povidone-iodine and a gauze dressing with plaster. |
Timeline
- Start date
- 2018-06-01
- Primary completion
- 2022-12-01
- Completion
- 2022-12-01
- First posted
- 2020-06-09
- Last updated
- 2020-06-09
Locations
1 site across 1 country: Spain
Source: ClinicalTrials.gov record NCT04422119. Inclusion in this directory is not an endorsement.