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

NCT02284373 · Status: TERMINATED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 39

Last updated 2020-03-13

Study results available
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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.

Conditions

  • Lymphedema

Interventions

OTHER

Flexitouch for 1 month in addition to routine wound care

simultaneous wound care and pneumonic compression

OTHER

Routine wound care for venous ulcers and lymphedema

wound care /dressings

DEVICE

Flexitouch pneumonic compression

pneumonic compression only

Sponsors & Collaborators

Study Design

Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
NONE
Model
PARALLEL

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2011-05-31
Primary Completion
2014-09-30
Completion
2014-10-31

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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 NCT02284373 on ClinicalTrials.gov