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Radial Medical - GAPS

NCT04163913 · Status: WITHDRAWN · Phase: NA · Type: INTERVENTIONAL

Last updated 2020-10-28

No results posted yet for this study

Summary

This study will prospectively compare compliance rates between a novel FDA cleared wearable compression therapy with and without digital engagement for DVT prophylaxis in both hospital and home environments after total knee or hip arthroplasty.

Conditions

Interventions

OTHER

Change in User interfaces of Cirvo compression device application.

Comparison of 2 versions of the Circo user interface

OTHER

Change in Satisfaction in use of Cirvo device

Comparison of how satisfied patients are with the Cirvo device to a different compression device (ActiveCare)

Sponsors & Collaborators

Principal Investigators

  • James Slover, MD · NYU Langone Health

Study Design

Allocation
RANDOMIZED
Purpose
SUPPORTIVE_CARE
Masking
NONE
Model
SINGLE_GROUP

Eligibility

Min Age
18 Years
Max Age
99 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2019-11-30
Primary Completion
2020-06-30
Completion
2022-06-30

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT04163913 on ClinicalTrials.gov