Trials / Unknown
UnknownNCT00146666
Evaluation of FM220 in Patients With Peripheral Arterial Disease (PAD)
- Status
- Unknown
- Phase
- Phase 2
- Study type
- Interventional
- Enrollment
- 90 (estimated)
- Sponsor
- FlowMedic · Industry
- Sex
- All
- Age
- 40 Years
- Healthy volunteers
- Not accepted
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.
Conditions
Interventions
| Type | Name | Description |
|---|---|---|
| DEVICE | Intermittent compression |
Timeline
- Start date
- 2005-09-01
- Completion
- 2006-09-01
- First posted
- 2005-09-07
- Last updated
- 2009-12-17
Locations
2 sites across 1 country: United States
Source: ClinicalTrials.gov record NCT00146666. Inclusion in this directory is not an endorsement.