Last updated on November 2016

Randomized Trial Comparing a Dual Action Pneumatic Compression System against Multi-Layer Bandaging Systems: A non-inferiority study


Brief description of study

Randomized Trial Comparing a Dual Action Pneumatic Compression System against Multi-Layer Bandaging Systems: A non-inferiority study

Detailed Study Description

The purpose of this study is to examine the effects of the ACTitouch® Adaptive Compression in healing venous leg ulcers compared to multi-layer bandaging wraps such as PROFORE and Coban™ 2. The ACTitouch device has been cleared by the Food and Drug Administration (FDA) and is available with a prescription from your doctor.

Clinical Study Identifier: TX146119

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