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A prospective study for the assessment of recurrence risk in stage II colon cancer patients using ColoPrint.

A prospective study for the assessment of recurrence risk in stage II colon cancer patients using ColoPrint. - PARSC

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
NL-OMON
Registry ID
NL-OMON31942
Enrollment
100
Registered
2008-10-03
Start date
2008-07-01
Completion date
Unknown
Last updated
2024-05-06

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

Conditions

adenocarcinoma of the colon colon cancer

Interventions

None listed

Sponsors

Agendia B.V.
Lead Sponsor

Eligibility

Age
18 Years to 99 Years

Inclusion criteria

Inclusion criteria: - > 18 - adenocarcinoma of the colon - stage II (1-III) planned to be treated with radical surgery

Exclusion criteria

Exclusion criteria: - prior malignancy with the exception of basal cell carcinoma or cervical dysplasia - any neo-adjuvant therapy - synchronous tumors

Design outcomes

Primary

MeasureTime frame
• Endpoint: risk assessment by Physician (based on local protocol) in comparison with ColoPrint result • Endpoint: relapse or 3 years disease-free survival (DFS)

Secondary

MeasureTime frame
-

Countries

Netherlands

Outcome results

None listed

Source: NL-OMON (via WHO ICTRP)