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Evaluation of a Dual Action Pneumatic Compression Device: Patient Ease of Use and Comfort

Chronic Venous Insufficiency Clinical Trial

Official title:
Evaluation of a Dual Action Pneumatic Compression Device: Patient Ease of Use and Comfort

Clinical Trial Summary

The purpose of this study is to determine the ease of use and comfort of the ACTitouch dual action pneumatic compression device in patients with unilateral or bilateral chronic venous insufficiency (CVI) with or without venous leg ulcers, as compared to standard compression.

Clinical Trial Description

Subjects will be randomized to receive either the ACTitouch system or standard compression garments, and will respond to symptom surveys and quality of life surveys to assess comfort and ease of use of each. These will be conducted at Baseline, at Day 15 and Day 30. ;

Study Design

Allocation: Randomized, Intervention Model: Parallel Assignment, Masking: Open Label

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT02015221
Study type Interventional
Source Tactile Medical
Contact
Status Completed
Phase N/A
Start date November 2013
Completion date June 2015
View Details
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