D-dimer Levels During and After Anticoagulation in Patients With a Previous Venous Thromboembolism: Effects on the Risk of Recurrence

This study has been completed.
Sponsor:
Collaborator:
Italian Federation of Anticoagulation Clinics (FCSA)
Information provided by (Responsible Party):
GUALTIERO PALARETI, St. Orsola Hospital
ClinicalTrials.gov Identifier:
NCT00266045
First received: December 13, 2005
Last updated: August 31, 2012
Last verified: August 2012

December 13, 2005
August 31, 2012
August 2005
June 2008   (final data collection date for primary outcome measure)
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Complete list of historical versions of study NCT00266045 on ClinicalTrials.gov Archive Site
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D-dimer Levels During and After Anticoagulation in Patients With a Previous Venous Thromboembolism: Effects on the Risk of Recurrence
A Multicentre, Prospective, Observational Study on the Predictive Role for Recurrence of D-dimer Levels Measured During and After Anticoagulation in Patients With a First Venous Thromboembolism Episode (the PROLONG-II Study)

The results of the Prolong study, currently submitted for publication, show that patients with a first unprovoked venous thromboembolic event who have altered D-dimer levels, measured one month after anticoagulation with vitamin K antagonists is stopped, have a high rate of recurrences (about 14%) and a prolongation of anticoagulation is effective in reducing significantly this rate. Those patients with normal D-dimer (about 60% of all patients examined) have a low rate of recurrences (about 5%) and likely a prolongation of anticoagulation in all these patients cannot be recommended.

In line with these results, the Prolong-Two study aims at assessing the predictive role for recurrence of D-dimer levels measured: a) during anticoagulation, b) one month after its withdrawal and c) periodically during follow up.

Patients with a first unprovoked venous thromboembolism (including proximal deep vein thrombosis of a leg and/or pulmonary embolism) which are treated with vitamin K antagonists for not less than 6 months are considered for the study. D-dimer assay is performed during anticoagulation and patients with altered results continue the anticoagulation for 6 more months. Those with normal D-dimer stop the anticoagulant treatment and are again examined one month later. Anticoagulation is resumed for 6 more months in those patients with abnormal D-dimer results but is permanently stopped in those with a normal assay. The latter patients are examined and D-dimer assay performed again every two months to evaluate the natural history of the assay after anticoagulation is stopped and the possible predictive value for recurrence of a change of the assay during follow-up from normal to abnormal results.

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Observational
Observational Model: Cohort
Time Perspective: Prospective
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Retention:   Samples Without DNA
Description:

Plasma samples for D-dimer assays or other coagulation tests

Probability Sample

Subjects with a single previous idiopathic venous thromboembolic event who stop anticoagulation

  • Deep Vein Thrombosis
  • Pulmonary Embolism
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*   Includes publications given by the data provider as well as publications identified by ClinicalTrials.gov Identifier (NCT Number) in Medline.
 
Completed
355
December 2008
June 2008   (final data collection date for primary outcome measure)

Inclusion Criteria

  • Age > 18 years
  • After a first documented idiopathic proximal deep vein thrombosis and/or pulmonary embolism
  • After at least 6 months of oral anticoagulation
  • After written informed consent

Exclusion Criteria:

  • Age > 82 y
  • Recurrent venous thromboembolism
  • 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
Both
18 Years to 82 Years
No
Contact information is only displayed when the study is recruiting subjects
Italy
 
NCT00266045
PROLONG-TWO STUDY
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GUALTIERO PALARETI, St. Orsola Hospital
St. Orsola Hospital
Italian Federation of Anticoagulation Clinics (FCSA)
Study Chair: Gualtiero Palareti, MD Dept. Angiology & Blood Coagulation, University Hospital S. Orsola-Malpighi, Bologna
St. Orsola Hospital
August 2012

ICMJE     Data element required by the International Committee of Medical Journal Editors and the World Health Organization ICTRP