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The Need for Compression Bandage Following Total Knee Arthroplasty A Prospective Randomized Controlled Trial Conducted in Simultaneous Bilateral Total Knee Replacements

Not Applicable
Completed
Conditions
Osteo Arthritis Knee
Interventions
Device: Gauze dressing
Device: Compression bandage
Registration Number
NCT03521869
Lead Sponsor
Rothman Institute Orthopaedics
Brief Summary

The purpose of this study is to evaluate if applying a compression bandage on the leg alters early outcome following TKA.

The primary objective of this study is to evaluate leg swelling by measuring leg circumference following simultaneous bilateral total knee arthroplasty (TKA) with and without the application of compression bandage.

Detailed Description

Not available

Recruitment & Eligibility

Status
COMPLETED
Sex
All
Target Recruitment
50
Inclusion Criteria
  • All patients receiving elective simultaneous bilateral primary total knee arthroplasty, treated by Rothman physicians at the Thomas Jefferson University Hospital or Rothman Specialty Hospital.
Exclusion Criteria
  • Previous venous thromboembolic event.
  • Lymph edema in one or both legs.
  • BMI > 40
  • Prior surgery (other than arthroscopy)

Study & Design

Study Type
INTERVENTIONAL
Study Design
PARALLEL
Arm && Interventions
GroupInterventionDescription
Standard gauze groupGauze dressing-
Compression bandage groupCompression bandage-
Primary Outcome Measures
NameTimeMethod
swelling of the kneeone day following surgery

Swelling of the leg will be determined by measuring circumference of the leg

Secondary Outcome Measures
NameTimeMethod

Trial Locations

Locations (1)

Rothman Institute

🇺🇸

Philadelphia, Pennsylvania, United States

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