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Cancer-related Venous Thromboembolic Disease - Cohort Study (CAPE)

R

Regional University Hospital Center (CHRU)

Status

Not yet enrolling

Conditions

Thromboses, Venous
Cancer
Thrombosis Embolism

Treatments

Other: Collection of biological samples

Study type

Observational

Funder types

Other

Identifiers

NCT06393764
29BRC21.0290

Details and patient eligibility

About

Venous thromboembolic disease (VTE) is a common (1/1000), potentially serious disease (10% mortality when the clinical presentation is that of pulmonary embolism (PE)). In cancer patients, the risk of developing VTE is high and constitutes a negative prognostic factor for cancer; the risk of bleeding is also increased. The study of VTE in the context of cancer is a major challenge, given the frequency of the association, the heterogeneity of the situations, the risk factors involved and the therapeutic issues in both curative and primary prevention; in this field, many uncertainties remain, justifying a study focused on the association of VTE and cancer.

Full description

Cancer is associated with a higher risk of VTE and mortality. This association is characterized by various uncertainties at pathophysiological, diagnostic, therapeutic and prognostic levels.

CAPE STUDY is a prospective, single-center interventional cohort follow-up study designed to investigate the risk of recurrence of VTE and its mechanisms in cancer patients.

The study involves the collection of biological samples from cancer patients with venous thromboembolic disease.

At inclusion and in case of recurrence of thrombosis or hemorrhage:

  • Blood samples will be taken for analysis and to constitute a biobank for future assays.
  • Urine samples will be collected Once a year for 5 years (and adapted to the clinical context): visit as part of routine care, or mailing of a questionnaire, or telephone contact.

Enrollment

150 estimated patients

Sex

All

Ages

18 to 80 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Patients aged 18 years and more.
  • Patients with active cancer or requiring cancer treatment at the time of their VTE episode
  • Patients with documented VTE less than 2 years old
  • Patients affiliated to the social security system
  • Patient who has signed a written informed consent

Exclusion criteria

  • Patient under 18
  • Refusal to participate
  • Incapacity to consent to the study
  • Patient under guardianship
  • Incapacity to communicate (comprehension disorder)
  • Life expectancy of less than 6 months

Trial design

150 participants in 1 patient group

Cancer patients treated for MVTE
Description:
All the patients are included in one arm. They will undergo various type of samples.
Treatment:
Other: Collection of biological samples

Trial contacts and locations

0

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Central trial contact

Françis Couturaud, Pr

Data sourced from clinicaltrials.gov

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