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D-dimer to Establish Duration of Anticoagulation After Venous Thromboembolism

Primary Purpose

Deep Vein Thrombosis, Pulmonary Embolism

Status
Completed
Phase
Phase 4
Locations
Italy
Study Type
Interventional
Intervention
Vitamin K antagonist (Coumarin anticoagulants)
Sponsored by
IRCCS Azienda Ospedaliero-Universitaria di Bologna
About
Eligibility
Locations
Outcomes
Full info

About this trial

This is an interventional treatment trial for Deep Vein Thrombosis focused on measuring D-dimer, Recurrence, Venous Thromboembolism, Anticoagulation, Duration

Eligibility Criteria

18 Years - undefined (Adult, Older Adult)All SexesDoes not accept healthy volunteers

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

Sites / Locations

  • Dept. of Angiology & Blood Coagulation, University Hospital S. Orsola-Malpighi

Outcomes

Primary Outcome Measures

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

Secondary Outcome Measures

Full Information

First Posted
December 9, 2005
Last Updated
March 18, 2021
Sponsor
IRCCS Azienda Ospedaliero-Universitaria di Bologna
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1. Study Identification

Unique Protocol Identification Number
NCT00264277
Brief Title
D-dimer to Establish Duration of Anticoagulation After Venous Thromboembolism
Official Title
D-dimer Test to Establish Duration of Anticoagulation After a First Idiopathic Episode of Venous Thromboembolism; the Prospective Randomized "Prolong" Study
Study Type
Interventional

2. Study Status

Record Verification Date
March 2021
Overall Recruitment Status
Completed
Study Start Date
September 2002 (undefined)
Primary Completion Date
December 2004 (Actual)
Study Completion Date
September 2005 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
IRCCS Azienda Ospedaliero-Universitaria di Bologna

4. Oversight

5. Study Description

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.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Deep Vein Thrombosis, Pulmonary Embolism
Keywords
D-dimer, Recurrence, Venous Thromboembolism, Anticoagulation, Duration

7. Study Design

Primary Purpose
Treatment
Study Phase
Phase 4
Interventional Study Model
Parallel Assignment
Masking
None (Open Label)
Allocation
Randomized
Enrollment
600 (false)

8. Arms, Groups, and Interventions

Intervention Type
Drug
Intervention Name(s)
Vitamin K antagonist (Coumarin anticoagulants)
Primary Outcome Measure Information:
Title
Confirmed recurrent proximal deep vein thrombosis and/or pulmonary embolism at 18 months follow up
Title
Confirmed major bleeding events at 18 months follow up

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
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
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
GUALTIERO PALARETI, MD
Organizational Affiliation
Head of Dept. Angiology & Blood Coagulation, University Hospital S. Orsola-Malpighi, Bologna, Italy
Official's Role
Study Chair
Facility Information:
Facility Name
Dept. of Angiology & Blood Coagulation, University Hospital S. Orsola-Malpighi
City
Bologna
State/Province
BO
ZIP/Postal Code
40138
Country
Italy

12. IPD Sharing Statement

Citations:
PubMed Identifier
11848459
Citation
Palareti G, Legnani C, Cosmi B, Guazzaloca G, Pancani C, Coccheri S. Risk of venous thromboembolism recurrence: high negative predictive value of D-dimer performed after oral anticoagulation is stopped. Thromb Haemost. 2002 Jan;87(1):7-12.
Results Reference
background
PubMed Identifier
12847064
Citation
Palareti G, Legnani C, Cosmi B, Valdre L, Lunghi B, Bernardi F, Coccheri S. Predictive value of D-dimer test for recurrent venous thromboembolism after anticoagulation withdrawal in subjects with a previous idiopathic event and in carriers of congenital thrombophilia. Circulation. 2003 Jul 22;108(3):313-8. doi: 10.1161/01.CIR.0000079162.69615.0F. Epub 2003 Jul 7.
Results Reference
background
PubMed Identifier
12941680
Citation
Eichinger S, Minar E, Bialonczyk C, Hirschl M, Quehenberger P, Schneider B, Weltermann A, Wagner O, Kyrle PA. D-dimer levels and risk of recurrent venous thromboembolism. JAMA. 2003 Aug 27;290(8):1071-4. doi: 10.1001/jama.290.8.1071.
Results Reference
background
PubMed Identifier
17065639
Citation
Palareti G, Cosmi B, Legnani C, Tosetto A, Brusi C, Iorio A, Pengo V, Ghirarduzzi A, Pattacini C, Testa S, Lensing AW, Tripodi A; PROLONG Investigators. D-dimer testing to determine the duration of anticoagulation therapy. N Engl J Med. 2006 Oct 26;355(17):1780-9. doi: 10.1056/NEJMoa054444. Erratum In: N Engl J Med. 2006 Dec 28;355(26):2797.
Results Reference
result
PubMed Identifier
23306310
Citation
Cosmi B, Legnani C, Pengo V, Ghirarduzzi A, Testa S, Poli D, Prisco D, Tripodi A, Palareti G; PROLONG Investigators (on behalf of FCSA, Italian Federation of Anticoagulation Clinics). The influence of factor V Leiden and G20210A prothrombin mutation on the presence of residual vein obstruction after idiopathic deep-vein thrombosis of the lower limbs. Thromb Haemost. 2013 Mar;109(3):510-6. doi: 10.1160/TH12-01-0041. Epub 2013 Jan 10.
Results Reference
derived
PubMed Identifier
20553388
Citation
Cosmi B, Legnani C, Tosetto A, Pengo V, Ghirarduzzi A, Testa S, Prisco D, Poli D, Tripodi A, Palareti G; Prolong Investigators. Sex, age and normal post-anticoagulation D-dimer as risk factors for recurrence after idiopathic venous thromboembolism in the Prolong study extension. J Thromb Haemost. 2010 Sep;8(9):1933-42. doi: 10.1111/j.1538-7836.2010.03955.x.
Results Reference
derived
PubMed Identifier
20352167
Citation
Cosmi B, Legnani C, Tosetto A, Pengo V, Ghirarduzzi A, Testa S, Prisco D, Poli D, Tripodi A, Palareti G; PROLONG Investigators; FCSA, Italian Federation of Anticoagulation Clinics. Comorbidities, alone and in combination with D-dimer, as risk factors for recurrence after a first episode of unprovoked venous thromboembolism in the extended follow-up of the PROLONG study. Thromb Haemost. 2010 Jun;103(6):1152-60. doi: 10.1160/TH09-11-0759. Epub 2010 Mar 29.
Results Reference
derived

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D-dimer to Establish Duration of Anticoagulation After Venous Thromboembolism

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