Status:

TERMINATED

Randomized Clinical Trial of Pneumatic Compression Device for the Treatment of Venous Ulcers and Lymphedema

Lead Sponsor:

NYU Langone Health

Conditions:

Lymphedema

Eligibility:

All Genders

18+ years

Phase:

NA

Brief Summary

The purpose of this study is to evaluate the effect of pneumatic compression in improving symptoms, quality of life and wound healing in patients with venous ulcers and/or lymphedema.

Detailed Description

This investigation is a randomized clinical trial of a prospective cohort of an estimated 140 subjects with venous ulcers, with an observational cohort of 50 subjects with lymphedema. Venous ulcer sub...

Eligibility Criteria

Inclusion

  • Presence of a venous ulcer on the lower extremity for at least 12 weeks14 days
  • Presence of lymphedema in the lower extremity for at least 14 days

Exclusion

  • Pregnant women or women of childbearing potential not on contraception
  • Previous use of the pneumatic compression device
  • Class IV congestive heart failure

Key Trial Info

Start Date :

May 1 2011

Trial Type :

INTERVENTIONAL

Allocation :

ACTUAL

End Date :

October 1 2014

Estimated Enrollment :

39 Patients enrolled

Trial Details

Trial ID

NCT02284373

Start Date

May 1 2011

End Date

October 1 2014

Last Update

March 13 2020

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