Actively Recruiting

Age: 18Years +
All Genders
Healthy Volunteers
NCT06709846

Magnetic Resonance Imaging in Metabolic Diseases

Led by University of Ulm · Updated on 2026-02-13

126

Participants Needed

1

Research Sites

251 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

This study aims to leverage structural, functional, and metabolic magnetic resonance imaging (MRI) of the brain to identify imaging features that correlate with clinical parameters. It is hypothesized that individuals with metabolic diseases exhibit distinct functional and structural brain differences compared to healthy controls. These differences may evolve over time due to changes in whole-body metabolism or body weight, influenced by factors such as the natural progression of the disease or therapeutic interventions. Additionally, potential brain changes may correlate with body composition metrics, such as the fat content of specific body compartments. This is a prospective, single-center study conducted at Ulm University Hospital, designed to track the clinical and imaging histories of patients with metabolic diseases and compare them to healthy individuals. Eligible participants include adults (aged 18 and older) capable of providing informed consent. Recruitment will occur through routine clinical care or existing research studies. To provide a comprehensive understanding, the study will include both cross-sectional analyses and longitudinal follow-up of participants, integrating repeated assessments during routine medical visits.

CONDITIONS

Official Title

Magnetic Resonance Imaging in Metabolic Diseases

Who Can Participate

Age: 18Years +
All Genders
Healthy Volunteers

Eligibility Criteria

Eligible

You may qualify if you...

  • Patients with metabolic diseases or healthy control participants without metabolic diseases
  • Adults aged 18 years or older
  • Able to provide written informed consent
Not Eligible

You will not qualify if you...

  • History of traumatic brain injuries
  • Preterm birth (before 34th week of pregnancy)
  • History of brain surgery
  • Structural brain changes such as tumors or congenital abnormalities
  • Neurological developmental disorders including autism spectrum disorders, learning disabilities, or intellectual disability
  • Epilepsy
  • Drug addiction
  • Severe neurological or psychiatric disorders such as schizophrenia
  • Pregnancy
  • Acute clinically relevant inflammatory diseases
  • Acute systemic or local infections
  • Severe or unclear diseases as judged by the principal investigator
  • Pre-existing intellectual impairment
  • Significant difficulties in understanding language
  • Absence of written consent
  • General MRI exclusion criteria like having a pacemaker, neurostimulator, or cochlear implant

AI-Screening

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Trial Site Locations

Total: 1 location

1

University Hospital Ulm

Ulm, Germany, 89081

Actively Recruiting

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Research Team

M

Martin Heni, Prof. Dr. med.

CONTACT

N

Nico Sollmann, PD Dr. Dr. med.

CONTACT

How is the study designed?

Study Type

OBSERVATIONAL

Masking

N/A

Allocation

N/A

Model

N/A

Primary Purpose

N/A

Number of Arms

2

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