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Immediate Compression Garment for Total Knee Replacement
N/A
Waitlist Available
Led By Jason Jennings, MD
Research Sponsored by University of Colorado, Denver
Eligibility Criteria Checklist
Specific guidelines that determine who can or cannot participate in a clinical trial Must have
Scheduled to undergo a primary, unilateral total knee arthroplasty secondary to end-stage osteoarthritis
Be older than 18 years old
Timeline
Screening 3 weeks
Treatment Varies
Follow Up preoperatively, day 4 and weeks 1, 2, 3, and 6 postoperatively
Awards & highlights
Study Summary
This study is evaluating whether a compression garment may help reduce swelling after knee surgery.
Eligibility Criteria
Inclusion Criteria
You may be eligible if you check “Yes” for the criteria belowTimeline
Screening ~ 3 weeks3 visits
Treatment ~ Varies
Follow Up ~ preoperatively, day 4 and weeks 1, 2, 3, and 6 postoperatively
Screening ~ 3 weeks
Treatment ~ Varies
Follow Up ~preoperatively, day 4 and weeks 1, 2, 3, and 6 postoperatively
Treatment Details
Study Objectives
Outcome measures can provide a clearer picture of what you can expect from a treatment.Primary outcome measures
Change in total limb swelling from baseline to day 4 and weeks 1, 2, 3, and 6 postoperative
Secondary outcome measures
Adherence to the intervention as measured by self-report logs
Subject satisfaction as measured by a 5-point Likert scale ranging from "very unsatisfied" to "very satisfied"
Trial Design
1Treatment groups
Experimental Treatment
Group I: ICGExperimental Treatment1 Intervention
Immediate Compression Garment
Treatment
First Studied
Drug Approval Stage
How many patients have taken this drug
Immediate Compression Garment
2021
N/A
~30
Find a Location
Who is running the clinical trial?
mediUNKNOWN
1 Previous Clinical Trials
142 Total Patients Enrolled
University of Colorado, DenverLead Sponsor
1,738 Previous Clinical Trials
2,149,505 Total Patients Enrolled
Colorado Joint ReplacementOTHER
11 Previous Clinical Trials
3,200 Total Patients Enrolled
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