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Registry of Thrombosis & NEoplasia of Sociedad Española de Oncología Médica

Observational Epidemiological Study of Cancer-associated Thrombosis: Registry of Thrombosis & NEoplasia of SEOM (TESEO Study)

Status
Recruiting
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT03855592
Acronym
TESEO
Enrollment
700
Registered
2019-02-27
Start date
2018-07-04
Completion date
2026-07-31
Last updated
2025-05-16

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

Conditions

Cancer, Thromboembolism

Brief summary

Epidemiological, observational, non-interventional, multicentric study on patients diagnosed with cancer who develop a venous or arterial thromboembolic episode, symptomatic or incidental, within a month prior to cancer diagnosis or at anytime after such diagnosis

Interventions

None listed

Sponsors

Fundación Sociedad Española de Oncologia Médica
Lead SponsorOTHER

Study design

Observational model
OTHER
Time perspective
PROSPECTIVE

Eligibility

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

Inclusion criteria

* Over 18 years of age with a histologically confirmed diagnosis of malignant tumor. * Venous or arterial thromboembolism episode, symptomatic or incidental, in the month prior or any time after the cancer diagnosis and in the three previous months to enrollment, confirmed with an imaging technique: Doppler echocardiography, computed tomography (CT) angiography, etc. * Signing of informed consent.

Exclusion criteria

* Clinical diagnosis of thromboembolic event without radiological confirmation. * Presenting a single episode of superficial thrombophlebitis without association with another thromboembolic event. * Each patient will be recorded just once, and therefore a second thromboembolic event will be considered a rethrombosis and will be recorded as such. Patients with a rethrombosis and a previous thromboembolic event before the start of the study in each center will not be able to be included.

Design outcomes

Primary

MeasureTime frameDescription
Location of origin of the thromboembolytic eventBaselineDistribution in the number of patients according to the anatomical location affected by the thromboembolytic event.
Vessel of origin of the thromboembolytic eventBaselineDistribution in the number of patients according to the type of vessel affected by the thromboembolytic event.
Thromboembolytic event diagnosis typeBaselineProportion of patients with incidental versus symptomatic thormboembolic events
Primary tumor at the time of the thromboembolic eventBaselineDistribution of patients according to the organ affected by the primary tumor.
Tumor-Node-Metastasis classificationBaselineBased on the American Joint Committee on Cancer 2018 Tumor-Node-Metastasis classification system: T for extent or size of the tumor, N for lymph nodes spread and M for metastasis.
Time between cancer diagnosis and thromboembolic eventBaselineBased on date on confirmed diagnosis of cancer (primary tumor) and date of thromboembolic event
Patient situation at the last visit12 monthsNumber of patients with rethrombosis, bleeding, other complications, tumor progression or death.
Characteristics of treatment administered for cancerBaselineBased on the number of patients prescribed with chemotherapy, radiation therapy, hormonal therapy, erythropoietin, transfusions, surgery, catheter, etc.

Countries

Spain

Contacts

Primary ContactAndres Muñoz, M.D.
investigacion@mfar.net+34 93 434 44 12
Backup ContactFederico Nepote
investigacion@mfar.net+34 93 434 44 12

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026