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egative pressure wound therapy (NPWT) versus conventional wound dressings in Total Knee Arthroplasty

Not Applicable
Completed
Conditions
knee replacement
Musculoskeletal - Osteoarthritis
Registration Number
ACTRN12615001350516
Lead Sponsor
Orthopaedic Research institute of Queensland
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Completed
Sex
All
Target Recruitment
35
Inclusion Criteria

Patients undergoing Total knee Arthroplasty for treatment of knee Arthritis,
Male and non-pregnant females.

Exclusion Criteria

Previous joint replacement.
Known allergy to active ingredients in the drape adhesives used in dressings, both conventional dry dressings and Negative Pressure Wound Therapy devices.

Study & Design

Study Type
Interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Secondary Outcome Measures
NameTimeMethod
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