Ignite Creation Date:
2024-05-05 @ 5:17 PM
Last Modification Date:
2024-10-26 @ 9:30 AM
Study NCT ID:
NCT00426075
Status:
COMPLETED
Last Update Posted:
2008-06-10
First Post:
2007-01-23
Brief Title:
Full-Leg vs Below-Knee Elastic Stockings for Prevention of the Post-Thrombotic Syndrome
Sponsor:
University of Padova
Organization:
University of Padova
Study Overview
Official Title:
None
Status:
COMPLETED
Status Verified Date:
2008-06
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:
Prospective controlled randomized clinical trial Consecutive patients with acute proximal deep vein thrombosis of the lower extremities with or without contemporary manifestations of pulmonary embolism are randomized to receive either a below-knee or a full-leg graduated compression 30-40 mm Hg at the ankle elastic stocking for prevention of the post-thrombotic syndrome PTS All patients are followed up to three years to assess the development of the PTS defined according to a validated clinical score the Villalta scale The rate of PTS is compared between the two study groups In addition there is an assessment of patients compliance and tolerability of the two different devices
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