RecruitingNCT04238871

RaDiCo PID Cohort (RaDiCo-ILD Cohort in English)

Idiopathic Interstitial Pneumopathy : Genetic and Environmental Determinants From Infancy to Elderly


Sponsor

Institut National de la Santé Et de la Recherche Médicale, France

Enrollment

2,500 participants

Start Date

Jun 21, 2017

Study Type

OBSERVATIONAL

Conditions

Summary

The main objective is to describe the phenotypic features of the paediatric and adult patients with Idiopathic Interstitial Pneumopathy/Pneumopathy Interstitial Diffuse (IIP/PID), at diagnosis and during the follow-up. These data will be critical for the description of the natural history of the various forms of IIP/PID.


Eligibility

Inclusion Criteria5

  • Clinical criteria: chronic respiratory insufficiency manifestations including dyspnea/tachypnea, cough, and cyanosis during exercise or at rest
  • Radiological criteria: characteristic chest High-Resolution Computed Tomography (HRCT) abnormalities including widespread ground glass or alveolar attenuation, reticulation often associated with traction bronchiectasis, and honeycombing
  • Functional criteria: pulmonary function test abnormalities reflecting a restrictive pattern and including: loss of lung volume, vital capacity (VC), total lung capacity (TLC); reduction in the diffusion capacity of the lung for carbon monoxide (DLCO), gas exchange abnormalities, and altered ventilatory response to exercise
  • Patients (parents/guardians for paediatric/patients) having given an informed consent to participate in the protocol
  • Patients affiliated to the "Regime National d'Assurance Maladie"

Exclusion Criteria2

  • Patients with diffuse parenchymal lung diseases caused by drug toxicity, immunodeficiency, proliferative disorders including histiocytosis, and metabolic disorders
  • Patients (parents/guardians for paediatric patient) not able to approve/understand the protocol

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Locations(2)

CHU Lyon - Hôpital Louis Pradel

Bron, France

AP-HP - Hôpital Armand Trousseau

Paris, France

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NCT04238871