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Clinical Trials in Germany / NCT07300696
Recruiting Not applicable

Functional MRI for Monitoring Progression and Assessing Trends in ILD

NCT07300696 · tracked via the Priya Life Science Germany tracker
Phase
Not applicable
Started
2025-11-20
Last updated
2025-12-24

Condition(s) studied

Interstitial Lung Diseases (ILD)

Investigational drug(s) / intervention(s)

Lung MRI Protocol with Functional and Contrast-Enhanced Sequences

Lung MRI Protocol with Functional and Contrast-Enhanced Sequences: Participants will undergo a lung MRI protocol consisting of structural imaging, non-contrast functional imaging, and contrast-enhanced imaging. Some sequences are custom-developed and performed during free breathing to accommodate patients with respiratory limitations.

Study summary

The main objective of this study is to investigate the utility of functional MRI to differentiate, characterize, and monitor subgroups of ILD. This can be broken down into three specific objectives:

Determine if ILD features observed on high-resolution computed tomography (HRCT), such as ground glass opacities (GGO), are functionally different.

Analyse MRI metrics within each subgroup to determine whether these metrics distinguish different ILDs.

Assess MRI metrics longitudinally to see if these parameters change with disease progression, stability, or reversibility.

Eligibility

Sex
ALL
Min age
18 Years
Max age
—
Healthy volunteers
No
Inclusion Criteria: * Clinical indication for a routine HRCT because of either newly diagnosed idiopathic pulmonary fibrosis (IPF) or hypersensitivity pneumonitis (HP) or idiopathic non-specific interstitial pneumonia (iNSIP), suspected diagnosis, or follow-up * Capacity to consent * Ability to participate fully in the study (defined by the ability to lie still for the duration of imaging) Exclusion Criteria: * Pregnancy and breast feeding * Persons under the age of 18 and persons not able to give informed consent * Any medical conditions that could hinder the ability to adhere to the protocol * Any MRI contraindication, including previous allergic reactions to Gd-based MRI contrast material and renal dysfunction (eGFR \< 30 ml min/1,73 m2)

Primary outcome measure(s)

Trial sites (2)

FacilityCityRegionStatus
Thoraxklink Heidelberg - Universitätsklinikum Heidelberg Heidelberg Germany Recruiting
Universitätsklinikum Schleswig-Holstein, Campus Kiel Kiel Germany Active Not Recruiting

More University Hospital Heidelberg trials in Germany

Official registry record

This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View NCT07300696 on ClinicalTrials.gov ↗ ← All trials in Germany