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NCT07040189Recruiting

Gustabor Phase 1 - AI-based Creation of a Nutritional Plan to Compensate for Chemotherapy-induced Taste Disorders

Source: ClinicalTrials.gov · Last updated 21 Aug 2026

Brief summary (registry, in English)

The study investigates taste disorders that commonly occur during or after cancer treatment, often leading to issues such as malnutrition and treatment discontinuation. Although many non-pharmacological recommendations exist, it is unclear which methods are suitable for which individuals. This pilot study aims to use an AI-based, or rule-driven system to generate personalized recommendations based on patients' specific impairments and taste disorder. For the pilot study, the AI will be trained on recipes to create individualized meal plans, helping to identify foods that are likely to be better. The primary endpoint is the assessment of the nutritional intervention as helpful at the second visit within 12 weeks of inclusion.

Status (registry)
Recruiting
Study type
Interventional
Enrollment
51 (estimated)
First submitted
17 Jun 2025
Start date
25 Nov 2025
Primary completion date
31 Dec 2026
Lead sponsor
Wuerzburg University Hospital
NCT number
NCT07040189

What you commit to

  • Study type: Interventional
  • Planned participants: 51
  • From 25 Nov 2025 to the primary completion date, 31 Dec 2026
  • 3 sites in 1 country
  • Visits and tests: ask the trial team, the registry does not list them

Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.

Who cannot take part

Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.

Other illness

  • Taste disorder explained by other causes (e.g. existing before therapy or COVID disease)

Other

  • Pregnancy
  • Placement in an inpatient care facility

Who the study is looking for

  • Age ≥ 18
  • Suffering from one of the following tumor entities: Multiple myeloma or malignant tumor of the gastrointestinal tract
  • Mainly oral nutrition
  • Subjectively perceived tumor therapy-related taste disorder
  • At least two clinical presentations planned within 12 weeks with a minimum interval of three weeks
  • Ability to participate in nutritional intervention, including use of the online portal and implementation of recipe suggestions (e.g. resources and access to a kitchen), either independently or with third-party support (e.g. by relatives, outpatient care services).

Age in the registry: 18 years to - · Sex: All · Does not accept healthy volunteers

Full criteria on ClinicalTrials.gov

Sites (3)

Sites in registry order. Pick your city on the disease page to sort them by distance.

SiteCityCountrySite status
LMU Klinikum
Coordinator of this site? Confirm its status
MunichGermanyCompleted
Universitätsklinikum Regensburg
Coordinator of this site? Confirm its status
RegensburgGermanyRecruiting
Universitätsklinikum Würzburg
Coordinator of this site? Confirm its status
WürzburgGermanyRecruiting

This page is information, not medical advice. Discuss any trial with your doctor.