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In vivo study on the development and application of (real-time) MRI-based measurement methods

In vivo study on the development and application of (real-time) MRI-based measurement methods - MRI_method_development

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
DRKS
Registry ID
DRKS00040589
Enrollment
50
Registered
2026-06-09
Start date
2026-01-05
Completion date
Unknown
Last updated
2026-06-22

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Basic physiological study / Method development

Interventions

Group 1: Up to three hours of MRI scanning time for the development and optimization of MRI protocols for tracking food components and dosage forms, as well as for quantifying parameters in the digest

Sponsors

Universität Greifswald
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to No maximum

Inclusion criteria

Inclusion criteria: Age: 18 years or older Gender: Male and female Medical condition suitable for an MRI scan (to be assessed on a case-by-case basis by the study physician) Submission of a written informed consent form

Exclusion criteria

Exclusion criteria: • Disorders or conditions affecting the swallowing process (e.g., severe dysphagia related to food and/or solid oral medications) • Claustrophobia • Liver disease • Implanted or portable electromechanical medical devices such as pacemakers, defibrillators, or infusion pumps • Extensive dark tattoos • Known allergies or intolerances to the components of the liquids • Alcohol or drug addiction • Eating disorders such as anorexia, bulimia • Positive pregnancy test, pregnancy, or current desire to conceive • Individuals known to be unwilling or unable to reliably follow instructions • Individuals unable to understand written and verbal instructions and information regarding the study risks they will face • Less than 14 days after an acute illness • Systemic use of medications, particularly those that affect gastrointestinal function • Concurrent participation in interventional research studies; the interval since previous participation in other studies should not be less than 14 days

Design outcomes

Primary

MeasureTime frame
Development of methods for (real-time) MRI of the mouth, esophagus, and abdomen

Secondary

MeasureTime frame
Tracking of orally ingested liquids/food components and dosage forms in the gastrointestinal tract. Development of measurement protocols for future studies.

Countries

Germany

Contacts

Public ContactWerner Weitschies

Universität Greifswald

werner.weitschies@uni-greifswald.de+49 3834 4204813

Outcome results

None listed

Source: DRKS (via WHO ICTRP) · Data processed: Jun 29, 2026