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D-dimer to Establish Duration of Anticoagulation After Venous Thromboembolism

D-dimer Test to Establish Duration of Anticoagulation After a First Idiopathic Episode of Venous Thromboembolism; the Prospective Randomized Prolong Study

Status
Completed
Phases
Phase 4
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT00264277
Enrollment
600
Registered
2005-12-12
Start date
2002-09-30
Completion date
2005-09-30
Last updated
2021-03-19

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Deep Vein Thrombosis, Pulmonary Embolism

Keywords

D-dimer, Recurrence, Venous Thromboembolism, Anticoagulation, Duration

Brief summary

The optimal duration of oral anticoagulant treatment in patients with idiopathic venous thromboembolism is still uncertain. The present study addresses the possible role of the D-dimer test in assessing the need for continuation of anticoagulation.The study aims at assessing whether D-dimer assay may have a role in guiding the duration of anticoagulation in these patients

Detailed description

This is a multicenter prospective follow-up study in patients with a first episode of symptomatic idiopathic venous thromboembolism (proximal deep vein thrombosis and/or pulmonary embolism) who are treated with vitamin K antagonists (either warfarin or acenocoumarol) for a minimum of 3 months. Eligible patients who give informed consent are instructed to immediately stop oral anticoagulation and refrain from taking any other antithrombotic drugs until the next visit, scheduled after 30 days. At that visit, venous blood is sampled to perform D-dimer assay and thrombophilia tests. D-dimers are assessed using the Clearview Simplify D-dimer assay (Agen Biomedical Limited, Brisbane, Australia). Patients with normal D-dimer results do not continue anticoagulation, whereas those with elevated D-dimer results are randomized using a computer program to either stop or resume anticoagulation with vitamin K antagonists (INR 2.0-3.0). All patients are followed-up for 18 months. The study outcome are the composite of confirmed recurrent venous thromboembolism and major bleeding events. All suspected outcome events and all deaths are evaluated by a central adjudication committee whose members are unaware of the D-dimer and thrombophilia results and of the group assignments.

Interventions

DRUGVitamin K antagonist (Coumarin anticoagulants)

Sponsors

IRCCS Azienda Ospedaliero-Universitaria di Bologna
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* Age \> 18 years * After a first documented idiopathic proximal deep vein thrombosis and/or pulmonary embolism * After at least 3 months of oral anticoagulation * After written informed consent

Exclusion criteria

* If the Venous thromboembolism occurred: * during pregnancy or puerperium * after recent (i.e. within three months) fracture or plaster casting of a leg, * after immobilization with confinement to bed for three consecutive days * after surgery with general anesthesia lasting longer than 30 minutes * Patients with: * active cancer * antiphospholipid antibody syndrome * antithrombin deficiency * serious liver disease or renal insufficiency (creatininemia \> 2 mg/dL), * other indications for anticoagulation or contraindications for this treatment * limited life expectation * Patients who live too far from the clinical center

Design outcomes

Primary

MeasureTime frame
Confirmed recurrent proximal deep vein thrombosis and/or pulmonary embolism at 18 months follow up
Confirmed major bleeding events at 18 months follow up

Countries

Italy

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Apr 8, 2026