Skip to content

Screening for occult malignancy using 18F-Fluorodeoxyglucose Positron Emission Tomography/Computed Tomography (FDG PET/CT) in patients with unprovoked venous thromboembolism

Status
Active, not recruiting
Phases
Phase 3
Study type
Interventional
Source
EU CTIS
Registry ID
CTIS2024-514703-34-00
Acronym
29BRC20.0021
Enrollment
638
Registered
2024-06-18
Start date
2020-09-08
Completion date
Unknown
Last updated
2024-06-18

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

Conditions

Thromboembolic event, Cancer

Brief summary

Occult cancer “missed” by cancer screening defined as proven cancer diagnosed (either biopsy proven cancer or cancer diagnosis approved by adjudication committee in the absence of biopsy proven cancer) from the time of cancer screening completion to the end of the 1-year follow-up period, and not detected at the time of screening.

Detailed description

1) New cancer diagnosis after completion of the initial allocated screening strategy., 2) Early-stage (T1-2N0M0 as per the World Health Organization TNM classification system) and advanced-stage tumors at initial screening and during follow-up., 3) Cancer-related mortality during a 5-year follow-up period., 4) Diagnosis of cancer and costs from the viewpoint of the healthcare system over a one-year period in order to estimate the additional cost per additional cancer detected and the incremental cost utility ratio, 5) Additional tests following each strategy and during follow-up., 6) The data of this study will be used to develop a decision aid to assist future patients in the decision of cancer screening

Interventions

Sponsors

Centre Hospitalier Regional Et Universitaire De Brest
Lead SponsorOTHER

Eligibility

Sex/Gender
All
Age
18 Years to No maximum

Design outcomes

Primary

MeasureTime frame
Occult cancer “missed” by cancer screening defined as proven cancer diagnosed (either biopsy proven cancer or cancer diagnosis approved by adjudication committee in the absence of biopsy proven cancer) from the time of cancer screening completion to the end of the 1-year follow-up period, and not detected at the time of screening.

Secondary

MeasureTime frame
1) New cancer diagnosis after completion of the initial allocated screening strategy., 2) Early-stage (T1-2N0M0 as per the World Health Organization TNM classification system) and advanced-stage tumors at initial screening and during follow-up., 3) Cancer-related mortality during a 5-year follow-up period., 4) Diagnosis of cancer and costs from the viewpoint of the healthcare system over a one-year period in order to estimate the additional cost per additional cancer detected and the incremental cost utility ratio, 5) Additional tests following each strategy and during follow-up., 6) The data of this study will be used to develop a decision aid to assist future patients in the decision of cancer screening

Countries

France

Outcome results

None listed

Source: EU CTIS · Data processed: Feb 4, 2026