Clinical trial Recruiting at 1 site Observational Ages 18 to 70

Nutritional status monitoring for adults with gastroenteropancreatic neuroendocrine tumors

Official title: Nutritional Status Assessment in Adult Patients Followed for Gastroenteropancreatic Neuroendocrine Tumors at Strasbourg University Hospital

Run by University Hospital, Strasbourg, France · NCT07302100 · Data updated 2026-11-12

This project will see if nutrition problems are common and linked to outcomes in adults aged 18–70 being followed for gastroenteropancreatic neuroendocrine tumors at Strasbourg University Hospital.

More Gastroenteropancreatic Neuroendocrine Tumor trials

Quick facts

Study typeObservational
Ages18 Years to 70 Years
SexAll
Enrollment100 (estimated)
SponsorUniversity Hospital, Strasbourg, France
Academic / other
Drugs / interventionssunitinib, chemotherapy
Locations1 site (Strasbourg)
StatusRecruiting
StartedDecember 12, 2024
Main results expectedFebruary 2026
Study endsFebruary 2026
Registry record updatedDecember 24, 2025
Trial IDNCT07302100 on ClinicalTrials.gov

Is this trial a fit for you?

Likely a good fit

Adults aged 18 to 70 diagnosed with a gastric, pancreatic, or intestinal neuroendocrine tumor between 1 January 2000 and 30 November 2024 who are followed at the CHU de Strasbourg endocrine/nutrition service.

Probably not a fit

Patients outside the 18–70 age range, those not followed at CHU de Strasbourg, or those whose tumors were reclassified as non‑neuroendocrine by pathology are unlikely to receive direct benefit from participation.

A plain-English reading of the study's rules. Only the study team can confirm whether you qualify.

What this trial studies

This observational study will collect historical and current nutritional data from adults aged 18–70 who have been followed for gastroenteropancreatic neuroendocrine tumors at CHU de Strasbourg between 1 January 2000 and 30 November 2024. Investigators will record measures such as weight, body mass index, laboratory nutritional markers, and any documented nutritional interventions, and will relate these to tumor features and clinical outcomes. No experimental treatments are given; the protocol is descriptive and aims to characterize the prevalence and pattern of malnutrition in this patient group. Results are intended to inform nutritional screening and management pathways for patients with typically slow‑growing gastroenteropancreatic NETs.

Why it matters

Potential benefit: If successful, the study could help clinicians identify patients at risk of malnutrition earlier and guide nutritional care that may improve quality of life and clinical outcomes.

How similar studies have gone: Prior cancer research has shown that malnutrition predicts poorer outcomes and that nutritional interventions can improve results, but targeted evidence specifically for gastroenteropancreatic neuroendocrine tumors remains limited.

Who can join: the full rules

Show full inclusion / exclusion criteria
Inclusion Criteria:

* Adults aged 18 to 70 years
* Patients being monitored for a digestive neuroendocrine tumor (gastric, pancreatic, intestinal), diagnosed between January 1, 2000, and November 30, 2024

Exclusion Criteria:

\- Tumor reclassified as non-neuroendocrine by histopathology

Where it's running

  • Service d'Endocrinologie, Diabétologie, Nutrition - CHU de Strasbourg - France
    Strasbourg, France
    Recruiting

Study contacts

Similar studies

Other studies for the same condition or treatment. Recruiting studies are listed first.

How to take part

  1. Review the eligibility criteria above with your treating physician.
  2. Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
  3. Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.
Last reviewed 2026-11-14 by the Find a Trial editorial team. Information on this page is for educational purposes and is not medical advice. Always consult qualified healthcare professionals about clinical trial participation.