Clinical Trials Directory

Trials / Completed

CompletedNCT01258270

Efficacy and Patient Satisfaction With AQUACEL® Ag Surgical Dressing Compared to Standard Surgical Dressing

Efficacy and Patient Satisfaction With AQUACEL® Ag Surgical Dressing Compared to Standard Surgical Dressing. A Prospective, Randomized Study in Primary Total Joint Arthroplasty.

Status
Completed
Phase
N/A
Study type
Interventional
Enrollment
300 (actual)
Sponsor
OrthoCarolina Research Institute, Inc. · Academic / Other
Sex
All
Age
18 Years – 90 Years
Healthy volunteers
Not accepted

Summary

The objective of this study is to determine the safety and effectiveness of the AQUACEL® Ag Surgical Dressing (treatment group) as compared to prepackaged island wound dressings consisting of traditional tape and gauze (control group) for total hip and total knee arthroplasty.

Conditions

Interventions

TypeNameDescription
PROCEDUREPostop DressingThe AQUACEL® Ag Surgical Dressing is a silver impregnated, waterproof, adhesive dressing that sticks to the skin around the wound and blocks bacteria from the outside.
PROCEDUREPostop DressingA standard island dressing consists of adhesive tape and gauze.

Timeline

Start date
2010-12-01
Primary completion
2013-05-01
Completion
2013-05-01
First posted
2010-12-10
Last updated
2013-06-10

Locations

1 site across 1 country: United States

Source: ClinicalTrials.gov record NCT01258270. Inclusion in this directory is not an endorsement.