CI

At a glance

ClinicalIndex Comparison Record
N/ACompleted· 23 enrolled
Drug / intervention
Non-compressive Bioactive Garment +1 moredevice
Likely dose
Not stated in record
Structured eligibility isn't available for this trial yet — see the full criteria in the Eligibility tab below.

Standardized by ClinicalIndex from the ClinicalTrials.gov record · verify against the source.

Search/NCT04751942
NCT04751942N/ACompleted

Post-operative Comparison Between Standard Gradient Compression Dressing vs. Non-Compressive Bioactive Garment on Pain, Swelling and Range of Motion Following Total Knee Arthroplasty

University Hospitals Cleveland Medical Center·interventional·Posted Feb 12, 2021·Updated Nov 4, 2025

In Brief

A clinical study evaluating Non-compressive Bioactive Garment and thrombo-embolic deterrent for Osteoarthritis Knees Both. Completed, enrolled 23 participants across 1 site.

Detailed Summary

This prospective study will evaluate pain, swelling, ROM as well as narcotic use in post-operative total knee arthroplasty patients using novel Non-Compressive Bioactive Garment (NCBG) versus current standard of care gradient compression stocking (Thrombo-Embolic-Deterrent or TED hose). If NCBG proves to be more effective in these outcome areas, it will provide a new and comfortable way to reduce patient pain and swelling immediately following surgery

Study Details

Study Typeinterventional
Allocation--
Masking--
Primary Purpose--
CountriesUnited States
Collaborators--

Timeline

N/ACompletedFinished
202120222023202420252026
First PostedFeb 12, 2021
Enrollment StartOct 20, 2023
Primary CompletionJan 21, 2025
TodayJul 2, 2026
Enrollment to primary: 1.3 yearsPosted 5.4 years ago

Interventions

Non-compressive Bioactive Garmentdevice

patients will be assigned to wear the non-compressive bioactive garment following total knee arthroplasty

thrombo-embolic deterrentdevice

patients will be randomized to wear the gold standard TED hose following total knee arthroplasty