MedTrace Logo

A Preliminary Clinical Usability Study for the Recovery Force DVT II Cuff

NCT03328624 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 36

Last updated 2019-09-06

Study results available
· View outcomes & findings →

Summary

A preliminary clinical usability study to assess design, comfort, wearability, and acceptance of Recovery Force's Deep vein thrombosis (DVT) cuff

Conditions

  • Deep Vein Thrombosis
  • Venous Thrombosis

Interventions

DEVICE

Deep Vein Thrombosis (DVT) Cuff

Recovery Force's DVT II Cuff

Sponsors & Collaborators

  • Recovery Force LLC

    collaborator INDUSTRY

  • University of Southern California

    lead OTHER

Principal Investigators

  • David G Armstrong, DPM, MD, PhD · Professor of Surgery and Director, SALSA@USC

Study Design

Allocation
NA
Purpose
OTHER
Masking
NONE
Model
SINGLE_GROUP

Eligibility

Min Age
18 Years
Max Age
65 Years
Sex
ALL
Healthy Volunteers
Yes

Timeline & Regulatory

Start
2018-01-23
Primary Completion
2018-03-06
Completion
2018-04-25
FDA Device
Yes

Countries

  • United States

Study Locations

More Related Trials

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 NCT03328624 on ClinicalTrials.gov