Viewing Study NCT00437892



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Study NCT ID: NCT00437892
Status: TERMINATED
Last Update Posted: 2011-08-19
First Post: 2007-02-20

Brief Title: Statins to Reduce D-dimer Levels in Patients With Venous Thrombosis
Sponsor: Università degli Studi dellInsubria
Organization: Università degli Studi dellInsubria

Study Overview

Official Title: The Effect of Statins on D-dimer Levels in Patients With a Previous Venous Thromboembolic Event
Status: TERMINATED
Status Verified Date: 2011-08
Last Known Status: None
Delayed Posting: No
If Stopped, Why?: Competitive trials and slow recruitment rate
Has Expanded Access: False
If Expanded Access, NCT#: N/A
Has Expanded Access, NCT# Status: N/A
Acronym: None
Brief Summary: Elevated levels of D-dimer a marker of procoagulant state have been identified as a marker of an increased risk of recurrent VTE Statins have proven antithrombotic properties as suggested by the reduction of several prothrombotic markers including D-dimer in patients at high risk of arterial thrombosis Such antithrombotic properties could also be observed in patients at high risk of venous thrombosis Aim of the study is to assess the effect of statins on D-dimer levels in patients with previous VTE after oral anticoagulant treatment withdrawal
Detailed Description: Patients with a single episode of idiopathic VTE either DVT or pulmonary embolism who received at least 6 months of adequate treatment with oral anticoagulants for whom treatment withdrawal is planned and with LDL cholesterol levels of equal to or greater than 130 mgdL will be randomized to either atorvastatin 40 mg 1 tablet daily and lipid lowering diet or lipid lowering diet for 3 months On the day of oral anticoagulant treatment withdrawal Day 0 enrolled patients will undergo measurement of plasma D-dimer At 30 days 3 Day 30 patients will undergo measurement of D-dimer CK LDH ALAT e ASAT and clinical evaluation At 90 days 7 Day 90 patients will undergo measurement of D-dimer total cholesterol HDL cholesterol LDL cholesterol and triglycerides ed clinical evaluation CK LDH ALAT e ASAT At 6 months 1 Day 180 patients will undergo clinical evaluation

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