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Development of a Model to Predict the Risk of Venous Thromboembolic Events in Patients With Metastatic Bronchopulmonary Cancer

Développement d'un modèle prédictif du Risque de Survenue d'évènements Thromboemboliques Veineux Chez Les Patients Atteints de Cancer Broncho-pulmonaire métastatique

Status
UNKNOWN
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT04196790
Acronym
LUCAAT
Enrollment
500
Registered
2019-12-12
Start date
2019-12-18
Completion date
2021-12-18
Last updated
2019-12-20

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

Conditions

Metastatic Bronchopulmonary Cancer

Brief summary

Venous thrombo-embolism (VTE) is a frequent and serious complication of cancer. However, predictive tools for VTE in cancer patients is lacking. In patients with metastatic broncho-pulmonarycancer, biochemical characteristics might help to identify patients at high risk for VTE. The aim of this study is to derive a predictive score combining clinical and biochemical variable that predict VTE in metastatic broncho-pulmonary cancer.

Detailed description

Venous thrombo-embolism (VTE) is a frequent and serious complication of cancer. However, predictive tools for VTE in cancer patients is lacking. In patients with metastatic broncho-pulmonarycancer, biochemical characteristics might help to identify patients at high risk for VTE, particularly in adenocarcinoma. The aim of this study is to derive a predictive score combining clinical and biochemical variable that predict VTE in metastatic broncho-pulmonary cancer.

Interventions

None listed

Sponsors

University Hospital, Brest
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
PROSPECTIVE

Eligibility

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

Inclusion criteria

* metastatic broncho-pulmonary cancer * age ≥18 years * who are eligible for chemotherapy * non opposition obtained

Exclusion criteria

* age \<18 years * pregnancy, breast feeding * VTE in the past 6 months or at the time of cancer diagnosis * surgery in the past 3 months * refusal to participate

Design outcomes

Primary

MeasureTime frameDescription
venous thromboembolism at 12 months12 monthsobjectively diagnosed VTE based on validated diagnostic tests

Secondary

MeasureTime frameDescription
overall survivalone yearoverall survival
survival without progressionone yearsurvival without progression
VTE at 6 months6 monthsVTE at 6 months

Countries

France

Contacts

Primary ContactFrancis COUTURAUD
francis.couturuad@chu-brest.fr02-98-34-78-26

Outcome results

None listed

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