Clinical Trials Directory

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

TypeNameDescription
PROCEDUREMulti-Foam dressingApplication of a multi-layer foam dressing with Safetac in surgical wound
PROCEDUREUsual careCare 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.