Last updated on December 2009

Evaluation of FM220 in Patients With Peripheral Arterial Disease (PAD)


Brief description of study

The purpose of this study is to determine whether 12 weeks of daily home use of the FM220 in the most affected leg of patients with PAD and claudication, will improve peak walking time (PWT) at three months as compared with a non-treated control group.

Clinical Study Identifier: NCT00146666

.

Contact Investigators or Research Sites near you

Start Over

Please choose location

View all locations

Michael Koren, MD

Jacksonville Center for Clinical Research
Jacksonville, FL United States
  Connect »

Jeffrey M Martinez, MD

Peripheral Vascular Associates
San Antonio, TX United States
  Connect »