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Venous Thromboembolism in Advanced Lung Cancer

Real-world Study of the Incidence and Risk Factors of Venous Thromboembolism (VTE) in Chinese Advanced Stage Lung Cancer

Status
UNKNOWN
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT03581708
Acronym
RIVAL
Enrollment
1400
Registered
2018-07-10
Start date
2018-07-31
Completion date
2022-06-30
Last updated
2018-07-10

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

Conditions

Lung Neoplasms, Venous Thromboembolism

Keywords

lung cancer, Venous Thromboembolism

Brief summary

This is a prospective observatory clinical study, aiming to establish and validate venous thromboembolism risk model in Chinese advanced non-small cell lung cancer.

Detailed description

VTE has high incidence in lung cancer and increases the mortality. Appropriate preventive measures contribute to 50% increase of incidence. The investigators are to investigate the VTE in advanced non-small cell lung cancer and delineate the risk factors to establish a VTE risk model system helping clinicians to differentiate VTE high risk population and apply early prevention in order to reduce the incidence of VTE.

Interventions

OTHERlung cancer

If the patient is diagnosed with lung cancer in advanced stage, he/she will be followed up for VTE incidence

Sponsors

Guangdong Provincial People's Hospital
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

* Age ≥ 18 years at the time of screening. * Eastern Cooperative Oncology Group performance status of ≤ 2. * Written informed consent obtained from the patient. * Histologically and cytologically documented Stage 3B-4 lung cancer (according to Version 8 of the International Association for the Study of Lung Cancer Staging system). * Patients with stage 1 to 3, who undergo radical therapy with disease free survival (DFS) \>12 months. * Willingness and ability to comply with scheduled visits and other study procedures.

Exclusion criteria

* History of another primary malignancy except for malignancy treated with curative intent with known active disease ≥ 5 years before date of the informed consent. * Without signed informed consent. * Unwillingness or inability to comply with scheduled visits or other study procedures. * Previously diagnosed with VTE before signing informed consent.

Design outcomes

Primary

MeasureTime frameDescription
VTE incidence risk evaluation12 monthsReal world VTE incidence risk evaluation in advanced lung cancer. Establish and validate VTE risk predictive model in Chinese advanced lung cancer.

Secondary

MeasureTime frameDescription
VTE incidence12 monthsVTE incidence in advanced lung cancer.
VTE and overall survival12 monthsThe influence on overall survival by VTE.

Countries

China

Contacts

Primary ContactZHEN WANG, PhD
hunterol@163.com862083827812
Backup ContactXIAOLING CHEN
chenxiaoling303@163.com8620-83827812

Outcome results

None listed

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