CompletedNot applicableNCT01727427

Prospective Study on the Treatment of Unsuspected Pulmonary Embolism in Cancer Patients

The same initial and long-term anticoagulation is suggested for unsuspected pulmonary embolism as for patients with symptomatic embolism. Based on these indications, cancer patients with unsuspected pulmonary embolism would be anticoagulated for at least 6 months or until the disease is active, which in most cases would mean indefinite treatment. In fact, dedicated studies on the treatment of unsuspected pulmonary embolism are missing, leaving doubts over the need for (indefinite) anticoagulation which exposes these patients to an increased risk of major bleeding events. Concerns over the need for anticoagulant treatment may especially hold for pulmonary embolism of the distal pulmonary tree since segmental and sub-segmental PE seem to have a more benign course than more proximal embolism. The scope of this study is to evaluate the current treatment approaches for unsuspected pulmonary embolism and to assess their efficacy and safety in a large prospective cohort of cancer patients.

Checked against the public recordLast updated Aug 8, 2019 · Source: ClinicalTrials.gov

StatusCompleted
PhaseNot applicable
U.S. locations46
SponsorG. d'Annunzio University
01
Study overview

What this study is about

Purpose
Not specified
Study type
Observational
Phase
Not applicable
Sponsor
G. d'Annunzio University
Interventions being studied
Drug: Heparin, fondaparinux, vitamin-K antagonists, aspirin
02
Explore related studies

How this study is categorized

These labels come from structured fields and exact terms in the public record.

03
Public criteria

Who may be able to participate

Inclusion Criteria: * cancer patients with a first diagnosis of unsuspected PE Exclusion Criteria: 1. age \<18 years; 2. ongoing anticoagulant therapy for previous VTE or indications for long-term anticoagulation other than deep vein thrombosis (DVT) or PE; 3. life expectancy less than 3 months.

Important: This is the sponsor’s public criteria, not a determination of eligibility. The study team must review your individual situation.

04
Study sites

U.S. locations

  • D.C. Veterans Affairs Medical CenterWashington D.C., District of Columbia
  • Clinical Division of Haematology, Department of Medicine IVienna
  • Division of Hematology, University of OttawaOttawa
  • CHU Amiens PicardieAmiens
  • Arras/Onco Nord Pas de Callais, LoosArras
  • Hopital Saint AndréBordeaux
  • Brest HIA Clermont TonnerreBrest
  • University hospital Centra La Cavale BlancheBrest
  • Montpellier et clinique du parc a Castelnau le nezCastelnau
  • Hopital G. Montpied Clermont-FerrandClermont
  • AP-HP Hopital Louis MourierColombes
  • Laboratoire d'Hématologie, DijonDijon

Source and freshness
Processed from ClinicalTrials.gov. Last public update: Aug 8, 2019. Always confirm current availability with the study team.

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