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Clinical Trials/NCT03189576
NCT03189576Active, not recruitingNot Applicable

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

Tampere University Hospital2 sites in 1 country37 target enrollmentStarted: October 1, 2015Last updated:
Conditions

Trial Snapshot

Phase
Not Applicable
Status
Active, not recruiting
Enrollment
37
Locations
2
Primary Endpoint
ctDNA level

Study 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.

Study Design

Study Type
Interventional
Allocation
Na
Intervention Model
Single Group
Primary Purpose
Diagnostic
Masking
None

Eligibility Criteria

Sex
All
Accepts Healthy Volunteers
Yes

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

Secondary Outcomes

No secondary outcomes reported

Investigators

Sponsor Class
Other
Responsible Party
Principal Investigator
Principal Investigator

Pirkko-Liisa Kellokumpu-Lehtinen

professor

Tampere University Hospital

Study Sites (2)

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