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Standard Dressing Versus Moist Dressing in the Course of the Postoperative Wound in Patients With Knee Prosthesis — APOSIT-PTG  

Surgical Wound Clinical Trial

Official title:
Standard Dressing Versus Moist Dressing in the Course of the Postoperative Wound in Patients With Knee Prosthesis

Clinical Trial 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

Clinical Trial 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%. ;

Study Design

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT04422119
Study type Interventional
Source Germans Trias i Pujol Hospital
Contact Sergio Alonso-Fernández, RN,MSN,PhD
Phone 0034934978437
Email salonso.germanstrias@gencat.cat
Status Recruiting
Phase N/A
Start date June 1, 2018
Completion date December 2022
View Details
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