Urine sensors could revolutionize cancer monitoring
NCT ID NCT01693835
First seen Jun 27, 2026 · Last updated Jun 27, 2026
Summary
This study tested whether special sensors could measure certain molecules in urine to track how cancer treatment is working. Researchers collected urine samples from 32 people with metastatic colorectal cancer and healthy volunteers over two days. The goal was to see if these molecules follow daily rhythms that could be used for non-invasive monitoring of cancer therapy.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- What this could lead to
- If successful, this could lead to a simple, non-invasive urine test to monitor how well cancer therapy is working, reducing the need for frequent biopsies or scans.
- What could go wrong
- This is a small, early observational study with only 32 participants, so results may not apply to all patients. The approach is still experimental and needs much more testing before it could be used in clinics.
This is an AI summary of the original study and may miss details. Read our disclaimer.
Study facts
What this study's own registry entry says, in plain language.
- Participants
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32 people
The number who actually took part.
- Start date
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Aug 2012
- Finished
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Jun 2014
- Lead sponsor
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A government agency
The lead sponsor is a government body.
Who can take part
This study's own entry requirements. Only the study team can say for certain whether you qualify.
Who is studied
Patients with metastatic colorectal cancer treated at the Department of Medical Oncology of Paul Brousse Hospital
- Ages
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18 years and older
- Sex
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Anyone
- Healthy volunteers
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Accepted
You do not need to have the condition being studied to take part.
Show the full entry requirements Hide the full entry requirements
Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.
Inclusion Criteria for patients: * Histologically-confirmed metastatic colorectal cancer; * 0 to 3 prior chemotherapy lines; * Signed informed consent; * Good understanding of the protocol and of the follow-up; * Estimated life expectancy exceeding 3 months; * At least one measurable metastatic lesion (RECIST criteria); * Performance Status (WHO) of 0 to 2; * Good haematological, hepatic and renal functions. Inclusion criteria for healthy subject * Age ≥ 18 ans * Signed informed consent; * Good understanding of the protocol and of the follow-up; * Good haematological, hepatic and renal functions. * Test HIV and B and C hepatitis negative test * No chronic or acute diseases Exclusion Criteria for patients: * Poor performance status (\>2); * Poor haematological, hepatic or renal functions; * Uncontrolled chronic disease; * Serious unhealed wound, ulcer or fracture within the previous month; * Clinical or laboratory finding suggesting possible abnormalities in nucleosides urinary excretion; * Pregnancy or breast-feeding during the previous month; * Transmeridian trip of more than 4 time zones within the prior 2 weeks; * Person with legal restriction to participate into clinical research, according to the current law in France. Exclusion criteria for healthy subject: * Poor haematological, hepatic or renal functions; * Uncontrolled chronic disease; * Serious unhealed wound, ulcer or fracture within the previous month; * Clinical or laboratory finding suggesting possible abnormalities in nucleosides urinary excretion; * Pregnancy or breast-feeding during the previous month; * Transmeridian trip of more than 4 time zones within the prior 2 weeks; * Person with legal restriction to participate into clinical research, according to the current law in France.
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Conditions
The condition(s) this trial relates to.
As listed by the trial registrant
The condition terms exactly as the trial's registrant entered them.
Contacts and locations
Locations
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Paul Brousse Hospital
Villejuif, 94800, France
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Other studies related to the condition(s) this trial covers.
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