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Clinical Trials in France / NCT07004595
Recruiting Observational

Evaluation of Frailty in Patients With Fibrosing Interstitial Lung Diseases: Prognostic and Therapeutic Impact

NCT07004595 · tracked via the Priya Life Science France tracker
Phase
Observational
Started
2025-07-20
Last updated
2026-06-24

Condition(s) studied

Sarcopenia

Investigational drug(s) / intervention(s)

Evaluation of patient frailty

Evaluation of patient frailty: Quality of Life questionnaire

Study summary

Fibrosing interstitial lung diseases (ILDs), with idiopathic pulmonary fibrosis being the most common form, primarily affect older individuals and have a poor prognosis, with a median survival of 3 to 5 years. While antifibrotic treatments such as nintedanib and pirfenidone can slow disease progression, their efficacy is often limited by side effects, particularly in elderly patients. A comprehensive patient assessment, including evaluations of frailty and sarcopenia, could optimize care by identifying those at risk for poor outcomes or poor treatment tolerance. Frailty, characterized by reduced physiological reserves, and sarcopenia, defined as a loss of muscle mass and strength, are both associated with increased mortality and morbidity risks. Although their individual impacts on fibrosing ILDs have been documented, the combined effect of these two syndromes on patient prognosis remains unexplored, highlighting the need for further studies to guide therapeutic decision-making.

Eligibility

Sex
ALL
Min age
65 Years
Max age
—
Healthy volunteers
No
Inclusion Criteria: * Patient with fibrosing ILD according to the ATS/ERS/JRS/ALAT 2022 criteria. * Patient aged ≥ 65 years. * Outpatient consultation (scheduled appointment in an outpatient clinic, day hospital, or weekly hospital stay). * French-speaking patient. * Patient who has received an information sheet explaining the study and has not expressed opposition to participating in this research. Exclusion Criteria: * Patient under legal guardianship, curatorship, or judicial protection. * Cognitive disorders limiting the use of questionnaires. * Patient with a CT scan showing an early usual interstitial pneumonia (UIP) pattern according to the ATS/ERS/JRS/ALAT 2022 classification.

Primary outcome measure(s)

Trial sites (1)

FacilityCityRegionStatus
CHU Nantes - Respiratory Department Nantes Nantes Recruiting

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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 NCT07004595 on ClinicalTrials.gov ↗ ← All trials in France