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

Status Recruiting

Clinical Trial Summary

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 Trial Description

n/a

Study Design

Allocation: Randomized, Endpoint Classification: Safety/Efficacy Study, Intervention Model: Parallel Assignment, Masking: Open Label, Primary Purpose: Treatment

Related Conditions & MeSH terms

Clinical Trial Details

NCT number	NCT00146666
Study type	Interventional
Source	FlowMedic
Contact	Yehudit Kraizer, Ph.D.
Phone	+972-54-3010902
Email	yehuditk@flowmedic.com
Status	Recruiting
Phase	Phase 2
Start date	September 2005
Completion date	September 2006

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