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Clinical Trial Details — Status: Recruiting

Administrative data

NCT number NCT03019471
Other study ID # NL55080.068.15
Secondary ID
Status Recruiting
Phase
First received
Last updated
Start date March 2016
Est. completion date December 2024

Study information

Verified date March 2023
Source Maastricht University Medical Center
Contact Merryn M. Macville, Dr.
Phone +31-43-3875843
Email m.macville@mumc.nl
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

The investigators aim to collect tumor DNA out of blood of cancer patients. If this is successful this could lead to the development of a cancer test in blood in the future, which is less invasive than current diagnostic methods.


Recruitment information / eligibility

Status Recruiting
Enrollment 40
Est. completion date December 2024
Est. primary completion date March 2024
Accepts healthy volunteers No
Gender All
Age group 18 Years and older
Eligibility Inclusion Criteria: 1. Patients with newly diagnosed local or metastatic breast cancer, colorectal cancer, non-small cell lung cancer and anaplastic glioblastoma, before start of radiation therapy, chemoradiation or chemotherapy. 2. Patients age > 18 years, willing and able to comply with the protocol as judged by the investigator with a signed informed consent Exclusion Criteria: 1. Patients with a history of malignant disease other than the disease under study, with an exception for adequately treated squamous cell carcinoma of the skin, basal cell carcinoma of the skin and in situ cervix carcinoma. 2. Pregnancy

Study Design


Related Conditions & MeSH terms


Intervention

Genetic:
Isolation of tumor DNA


Locations

Country Name City State
Netherlands Maastricht University Medical Center Maastricht Limburg

Sponsors (1)

Lead Sponsor Collaborator
Maastricht University Medical Center

Country where clinical trial is conducted

Netherlands, 

Outcome

Type Measure Description Time frame Safety issue
Primary ctDNA Demonstrate the presence or absence of ctDNA in patients plasma. Examine if there us a sufficient concentration of ctDNA in the plasma to reliably diagnose cancer and determine the CNV One year