Can a Dietitian's plan help older pancreatic cancer patients feel better?
NCT ID NCT07821554
First seen Sep 16, 2026 · Last updated Sep 17, 2026 · Updated 1 time
Summary
Researchers are testing whether personalised nutritional care from a trained dietitian improves quality of life for people aged 65 and older with pancreatic ductal adenocarcinoma. About 250 participants will be randomly assigned to either six months of individualised nutrition support or usual nutritional care. The study follows participants for 12 months and measures quality of life, weight, body composition, muscle strength, and physical function.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- Personalised nutritional care delivered by a trained dietitian, including dietary counselling, individual nutrition targets, and oral nutritional supplements when needed
- What this could lead to
- If it works, this could give older pancreatic cancer patients a structured way to maintain weight, muscle, and quality of life during treatment. It could also shape how cancer centres routinely support nutrition in this age group.
- What could go wrong
- Nutrition support may not be enough to counter the aggressive weight loss and muscle wasting that pancreatic cancer causes. The trial is open-label, so patients and dietitians know which group they are in, which can influence how people report their quality of life.
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.
- Phase
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Not a phased trial
Phase numbers describe drug development. The registry uses this when they do not apply, as it does for trials of devices, procedures or behaviour changes, and for observational studies.
- Participants
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About 250 people
The number the study aims to enrol. It can still change while the study runs.
- Expected to start
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Nov 2026
An estimate. Start dates often move.
- Expected to finish
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Aug 2030
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.
- Ages
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65 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: * Participant is 65 years or older at the time of signing informed consent. * Histologically or cytologically confirmed borderline resectable, locally advanced or metastatic pancreatic ductal adenocarcinoma. * Participant is managed at a participating oncology, surgical or gastroenterology site and is planned to start, or has recently started, an eligible PDAC treatment within 14 days. * ECOG performance status 0-2. * Signed informed consent before any study-specific procedure. Exclusion Criteria: * Expected life expectancy of less than 3 months, in the judgement of the investigator. * Unable to provide informed consent and no legally authorised representative procedure is applicable under local regulations. * Participation in another interventional nutrition trial or structured nutritional programme that would interfere with the NutriCa65 intervention or outcome assessments. * Known allergy, intolerance or contraindication to all available oral nutritional supplements or intervention products, where no suitable alternative can be provided. * Clinical condition making participation in trial procedures unsafe or excessively burdensome, as judged by the investigator. * Any other condition that, in the investigator's opinion, would compromise participant safety, rights or data integrity.
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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.
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
5 sites in 5 countries. 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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Department of Medical Oncology
Bucharest, Romania
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Department of Medical Oncology
Madrid, Spain
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Department of Medicine
Bergen, Norway
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Department of Oncology
Herlev, 2730, Denmark
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Department of Surgery, Oncology and Gastroenterology
Padova, Italy
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Other studies related to the condition(s) this trial covers.
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- Can a phone app help pancreatic cancer patients eat better during treatment?