Ignite Creation Date:
2024-05-05 @ 11:49 AM
Last Modification Date:
2024-10-26 @ 9:14 AM
Study NCT ID:
NCT00146666
Status:
UNKNOWN
Last Update Posted:
2009-12-17
First Post:
2005-09-03
Brief Title:
Evaluation of FM220 in Patients With Peripheral Arterial Disease PAD
Sponsor:
FlowMedic
Organization:
FlowMedic
Study Overview
Official Title:
Evaluation of FM220 in Patients With Peripheral Arterial Disease PAD
Status:
UNKNOWN
Status Verified Date:
2009-08
Last Known Status:
RECRUITING
Delayed Posting:
No
If Stopped, Why?:
Not Stopped
Has Expanded Access:
False
If Expanded Access, NCT#:
N/A
Has Expanded Access, NCT# Status:
N/A
Acronym:
None
Brief 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
Detailed Description:
None
Study Oversight
Has Oversight DMC:
None
Is a FDA Regulated Drug?:
None
Is a FDA Regulated Device?:
None
Is an Unapproved Device?:
None
Is a PPSD?:
None
Is a US Export?:
None
Is an FDA AA801 Violation?:
None