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Measuring Molecular Residual Disease in Colorectal Cancer After Primary Surgery and Resection of Metastases

Measuring Molecular Residual Disease in Colorectal Cancer After Primary Surgery and Resection of Metastases

Status
UNKNOWN
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT03189576
Enrollment
37
Registered
2017-06-16
Start date
2015-10-01
Completion date
2023-08-30
Last updated
2023-05-26

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

Conditions

Colorectal Cancer, Residual Disease

Brief summary

Circulating tumour DNA (ctDNA) is a promising tool when monitoring the residual disease in colorectal cancer (CRC). Current staging procedures are insufficient to identify the patient cohort at high risk, who might benefit from additional adjuvant therapy. We will show that the assessment of ctDNA is a non-invasive approach and easily taken at different time points via simple blood draw to monitor residual disease from the colorectal cancer patients after primary surgery. Minimal residual disease could be used in the future for individualized treatment decisions after primary surgery.

Interventions

DIAGNOSTIC_TESTblood draw

Sponsors

Tampere University Hospital
Lead SponsorOTHER

Study design

Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
DIAGNOSTIC
Masking
NONE

Eligibility

Sex/Gender
ALL
Healthy volunteers
Yes

Inclusion criteria

* planned colorectal primary surgery

Exclusion criteria

* unfit patients with dementia

Design outcomes

Primary

MeasureTime frameDescription
ctDNA level3-6 monthsresidual disease measured by sequential blood draws

Countries

Finland

Outcome results

None listed

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