ClinicalTrials.Veeva

Menu

Advanced Mutidimensional and Ultra High Resolution Computed Tomography to Inspect Cardiopulmonary Involvement in Progressive Fibrosing Interstitial Lung Diseases (AMICI-ILD)

S

San Donato Group (GSD)

Status

Enrolling

Conditions

Interstitial Lung Diseases

Study type

Observational

Funder types

Other

Identifiers

NCT06537934
PNRR-MCNT2- 2023-12377844

Details and patient eligibility

About

Interstitial lung diseases (ILDs) are common chronic disease characterized by high mortality and morbidity, also linked to cardiovascular implication. Cardiovascular complications, occur early in idiopathic pulmonary fibrosis (IPF) and other ILDs without anysymptoms. Symptoms are often misinterpreted and diagnosis delayed to irreversible stages of cardiac dysfunction. Mechanism of cardiac damage, the main cause of mortality, are heterogeneous raging from ischemic heart disease, acceleration of atherosclerosis, to right ventricle dysfunction secondary, to pulmonary hypertension. So an early recognition and accurate staging are fundamental to avoid disease progression and improve outcomes. The identification of a single non-invasive imaging modality able to simultaneously characterize in an accurate and quantitative way the entity of lung and cardiac damage in patients affected by ILD would be useful to improve risk stratification and to guide treatment.

Enrollment

123 estimated patients

Sex

All

Ages

18+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

• Adult subjects (>18 y.o.) with previously known ILD or high likelihood for having ILD including CTD diagnosis since at least 5 years before the project starts in order to increase the prevalence of ILD [2] who signed an Informed Consent authorizing data collection.

Exclusion criteria

  • Subjects with active infectious disease;
  • known CAD;
  • history of previous percutaneous or surgical revascularization;
  • known cardiomyopathy;
  • previous heart failure;
  • presence of cardiac devices (prosthetic valve, ICD, PM, ICD-CRT, LVAD)
  • previous or active neoplasia;
  • pregnancy and breastfeeding;
  • allergy to iodine contrast agent;
  • claustrophobia;
  • glomerular filtration rate < 30mL/min
  • impossibility to lay down or breath old
  • absence of informed consent signed

Trial contacts and locations

1

Loading...

Central trial contact

Antonio Esposito Esposito; Anna Palmisano

Data sourced from clinicaltrials.gov

Clinical trials

Find clinical trialsTrials by location
© Copyright 2026 Veeva Systems