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.
| Condition | Peripheral Arterial Disease, Intermittent Claudication |
|---|---|
| Treatment | Intermittent compression |
| Clinical Study Identifier | NCT00146666 |
| Sponsor | FlowMedic |
| Last Modified on | 22 January 2022 |
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