RECRUITINGOBSERVATIONAL
RaDiCo PID Cohort (RaDiCo-ILD Cohort in English)
Idiopathic Interstitial Pneumopathy : Genetic and Environmental Determinants From Infancy to Elderly
About This Trial
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.
Who May Be Eligible (Plain English)
Who May Qualify:
- 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 willing to sign a consent form to participate in the protocol
- Patients affiliated to the "Regime National d'Assurance Maladie"
Who Should NOT Join This Trial:
- Patients with diffuse parenchymal lung diseases caused by drug toxicity, weakened immune system, proliferative disorders including histiocytosis, and metabolic disorders
- Patients (parents/guardians for paediatric patient) not able to approve/understand the protocol
Always talk to your doctor about whether this trial is right for you.
Original Eligibility Criteria
View original clinical language
Inclusion Criteria:
* 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 Criteria:
* 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
Locations (2)
CHU Lyon - Hôpital Louis Pradel
Bron, France
AP-HP - Hôpital Armand Trousseau
Paris, France