Ignite Creation Date:
2024-05-05 @ 11:56 AM
Last Modification Date:
2024-10-26 @ 9:16 AM
Study NCT ID:
NCT00182208
Status:
COMPLETED
Last Update Posted:
2008-07-22
First Post:
2005-09-12
Brief Title:
Evaluation of a Venous-Return Assist Device Venowave to Treat Post-Thrombotic Syndrome A Randomized Controlled Trial
Sponsor:
Hamilton Health Sciences Corporation
Organization:
McMaster University
Study Overview
Official Title:
Evaluation of a Venous-Return Assist Device Venowave to Treat Post-Thrombotic Syndrome A Randomized Controlled Trial
Status:
COMPLETED
Status Verified Date:
2008-07
Last Known Status:
None
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 daily use of a lower limb venous-return assist device Venowave improves leg symptoms ability to perform activities of daily living and quality of life in subjects with severe PTS
Detailed Description:
Eligible consenting patients will be randomly allocated to receive either the veno-device active or placebo for 8 weeks and crossed over for a further 8 weeks active or placebo following a 4 week wash out period A randomized controlled crossover study
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
Secondary IDs
| Secondary ID | Type | Domain | Link |
|---|---|---|---|
| Health Canada No64844 | None | None | None |