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Clinical Trials/NCT03189576
NCT03189576
Active, not recruiting
Not Applicable

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

Tampere University Hospital1 site in 1 country37 target enrollmentOctober 1, 2015

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Colorectal Cancer
Sponsor
Tampere University Hospital
Enrollment
37
Locations
1
Primary Endpoint
ctDNA level
Status
Active, not recruiting
Last Updated
2 years ago

Overview

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.

Registry
clinicaltrials.gov
Start Date
October 1, 2015
End Date
August 30, 2023
Last Updated
2 years ago
Study Type
Interventional
Study Design
Single Group
Sex
All

Investigators

Responsible Party
Principal Investigator
Principal Investigator

Pirkko-Liisa Kellokumpu-Lehtinen

professor

Tampere University Hospital

Eligibility Criteria

Inclusion Criteria

  • planned colorectal primary surgery

Exclusion Criteria

  • unfit patients with dementia

Outcomes

Primary Outcomes

ctDNA level

Time Frame: 3-6 months

residual disease measured by sequential blood draws

Study Sites (1)

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