Gut bacteria may hold key to better nutrition for cancer patients
NCT ID NCT07260617
First seen Jun 26, 2026 · Last updated Jun 27, 2026 · Updated 1 time
Summary
This study looks at how the bacteria in the gut and mouth relate to nutrition in 150 adults with digestive cancer starting chemotherapy. Researchers will collect stool and saliva samples, along with questionnaires and tests, before and after the first chemo cycle. The goal is to find bacterial patterns linked to malnutrition, which could lead to new ways to support patients' nutrition during treatment.
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 identify gut bacteria as targets to improve nutrition and quality of life for cancer patients on chemotherapy.
- What could go wrong
- This is an early observational study, not a treatment trial. It may not find clear links, and any potential therapies would need years of additional testing.
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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About 150 people
The number the study aims to enrol. It can still change while the study runs.
- Expected to start
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Dec 2025
An estimate. Start dates often move.
- Expected to finish
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Dec 2027
An estimate. End dates often move.
- Lead sponsor
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Other sponsor
The registry's catch-all category, for sponsors it does not file as a company, a government agency, or a research network.
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 treated with chemotherapy in digestive oncology
- Ages
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18 years and older
- Sex
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Anyone
- Healthy volunteers
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Not accepted
This study is not open to healthy volunteers. The entry requirements below say who it is open to.
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 \* : * Adult patient * Patient with digestive cancer, including: * Borderline or locally advanced pancreatic adenocarcinoma * Metastatic pancreatic adenocarcinoma without symptomatic peritoneal carcinomatosis * metastatic colon/rectal cancer without symptomatic peritoneal carcinomatosis * Patients with an indication for chemotherapy (induction treatment or treatment of metastatic disease) * Patients able to eat orally at the time of inclusion in the study * Patients with a performance status (PS) score ≤2 * Patients who agree to provide stool and saliva samples * Patients who have given their written informed consent * Patients affiliated with the French social security system * Exclusion Criteria : * Pregnant or breastfeeding women * Patients who have received antibiotics within 3 weeks prior to the first chemotherapy treatment (excluding antibiotic prophylaxis administered in the context of surgery or endoscopy). * Individuals receiving psychiatric care that may interfere with their ability to respond to questionnaires (in the investigator's opinion) * Persons deprived of their liberty or subject to legal protection measures (guardianship, curatorship) * Patients participating in another interventional study with medication * Patients who have undergone chemotherapy for another malignant tumor in the last 12 months. * Patients with another synchronous malignant tumor, with the exception of adequately treated carcinoma in situ of the cervix or squamous cell carcinoma of the skin, or limited basal cell or squamous cell skin cancer. This cancer must then be adequately controlled. * Patients with symptomatic brain and/or meningeal metastases. * Patients who have undergone digestive resection (excluding appendectomy or cholecystectomy \>12 months ago). * Patients with symptomatic peritoneal carcinomatosis prior to the start of chemotherapy.
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Genom att skicka in godkänner du våra Användarvillkor
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.
How to take part
Only the study team decides who joins. These are the ways to reach them.
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The places running it
3 sites. The list below names each one and where it is.
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The official record
ClinicalTrials.gov lists the study team's own contact details, including names and phone numbers. We don't republish those.
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A doctor treating you
A doctor who knows your case can contact a study site on your behalf, and can tell you whether this study is worth pursuing at all.
Contacts and locations
Locations
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Croix Rousse Hospital Hepatology and Gastroenterology Department
Lyon, 69004, France
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Edouard Herriot Hospital - medical oncology department
Lyon, 69003, France
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Lyon Sud Hospital - Hepatology and Gastroenterology Department
Lyon, 69310, France
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