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Non-Invasive Management of Chronic Venous Insufficiency

NCT00950378 · Status: COMPLETED · Type: OBSERVATIONAL · Enrollment: 10

Last updated 2013-05-29

No results posted yet for this study

Summary

The purpose of this study is:

-item one to use two new non-invasive technologies to evaluate scarring and swelling associated with chronic venous insufficiency.

The study hypothesis:

\- item one non-invasive technologies can provide a tool for assessing risk of ulcer development based on the tissue edema and alteration.

Conditions

  • Venous Insufficiency

Sponsors & Collaborators

Principal Investigators

  • Harriet Hopf, MD · University of Utah

Eligibility

Min Age
40 Years
Max Age
60 Years
Sex
ALL
Healthy Volunteers
Yes

Timeline & Regulatory

Start
2009-07-31
Primary Completion
2012-08-31
Completion
2012-12-31

Countries

  • United States

Study Locations

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Entities

Companies

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 NCT00950378 on ClinicalTrials.gov