RaDiCo PID Cohort (RaDiCo-ILD Cohort in English)

NCT ID: NCT04238871

Last Updated: 2025-04-04

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

RECRUITING

Total Enrollment

2500 participants

Study Classification

OBSERVATIONAL

Study Start Date

2017-06-21

Study Completion Date

2026-12-31

Brief Summary

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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.

Detailed Description

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The French RaDiCo-PID : Idiopathic Interstitial Pneumopathy registry is an ongoing observational prospective and retrospective cohort with longitudinal long-term follow-up includes pediatric and adult patients with Idiopathic Interstitial Lung Disease (ILD) from the reference and competence centers.

Conditions

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Idiopathic Interstitial Pneumopathy/Pneumopathy Interstitial Diffuse Paediatric and Adult Patients

Study Design

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Observational Model Type

COHORT

Study Time Perspective

OTHER

Study Groups

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children or adults with Idiopathic Lung Disease

No interventions assigned to this group

Eligibility Criteria

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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
Eligible Sex

ALL

Accepts Healthy Volunteers

No

Sponsors

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

OTHER_GOV

Sponsor Role lead

Responsible Party

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Responsibility Role SPONSOR

Locations

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CHU Lyon - Hôpital Louis Pradel

Bron, , France

Site Status RECRUITING

AP-HP - Hôpital Armand Trousseau

Paris, , France

Site Status RECRUITING

Countries

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France

Central Contacts

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Marie Chevereau

Role: CONTACT

+ 33 1 71 73 87 94

Sonia Gueguen

Role: CONTACT

+33 6 88 34 54 08

Facility Contacts

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Vincent Cottin, Pr

Role: primary

Annick Clément, Pr

Role: primary

References

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Cottin V, Gueguen S, Nunes H, Jouneau S, Crestani B, Bonniaud P, Wemeau L, Israel-Biet D, Reynaud-Gaubert M, Gondouin A, Cadranel J, Marchand-Adam S, Chevereau M, Dufaure-Gare I, Amselem S, Clement A; and the RaDiCo team. Treatment of Idiopathic Pulmonary Fibrosis with Capsule or Tablet Formulations of Pirfenidone in the Real-Life French RaDiCo-ILD Cohort. Adv Ther. 2022 Jan;39(1):405-420. doi: 10.1007/s12325-021-01961-x. Epub 2021 Nov 10.

Reference Type DERIVED
PMID: 34757602 (View on PubMed)

Other Identifiers

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C15-64

Identifier Type: -

Identifier Source: org_study_id

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