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NCT03521869 Clinical Trial

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

Osteo Arthritis Knee Clinical Trial

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

Clinical Trial Details — Status: Completed

Administrative data
NCT number NCT03521869
Other study ID # 14WHoz
Secondary ID
Status Completed
Phase N/A
First received
Last updated
Start date November 13, 2014
Est. completion date June 2, 2017

Study information
Verified date April 2018
Source Rothman Institute Orthopaedics
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial 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.

Recruitment information / eligibility
Status Completed
Enrollment 50
Est. completion date June 2, 2017
Est. primary completion date June 2, 2017
Accepts healthy volunteers
Gender All
Age group 18 Years and older
Eligibility 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

Related Conditions & MeSH terms

Intervention

Device:
• Compression bandage
Compression bandage placed after total knee replacement
• Gauze dressing
standard of care gauze dressing placed after total knee replacement

Locations
Country Name City State
United States Rothman Institute Philadelphia Pennsylvania

Sponsors (1)
Lead Sponsor Collaborator
Rothman Institute Orthopaedics

Country where clinical trial is conducted

United States, 

Outcome
Type Measure Description Time frame Safety issue
Primary swelling of the knee Swelling of the leg will be determined by measuring circumference of the leg one day following surgery
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