DCP (RaDiCo Cohort) (RaDiCo-DCP)
Recruiting now
Conditions studied: Primary Ciliary Dyskinesia
In brief
Primary Ciliary Dyskinesias (PCD) are rare, autosomal recessive respiratory diseases, due to a defect in mucociliary clearance linked to abnormalities in the structure and/or function of the cilia. The variety of ciliary abnormalities identified reflects the genetic heterogeneity of PCDs. The thirty or so genes currently implicated explain the pathology in about half of the patients. PCDs are characterized by recurrent infections of the upper (rhinosinusitis) and lower (bronchitis) airways, beginning in early childhood and progressing respectively to nasal polyposis and bronchial dilatation. In half of the cases, there is a lateralization defect of the organs (situs inversus) corresponding to Kartagener's syndrome. There is more frequent infertility in men (immobility of spermatozoa) than in women (miscarriages and tubal pregnancies). About a third of patients progress to respiratory failure. The identification of predictive factors of severity, specific to PCDs, would improve patient care. It is also important to assess the quality of life of patients with PCD, particularly at the ENT level. Data from prevalent patients are currently integrated into three separate and complementary databases: the "e-RespiRare" database, the "DCP Cils" database and the "DCP genes" database. The first step is therefore to constitute the RaDiCo-DCP database which will include data from prevalent and incident patients whose diagnosis of PCD is certain. The cohort aims to improve the routine care of PCD patients, in particular by highlighting predictive factors of severity, allowing early and personalized care, to assess the social impact (quality of life) and medical conditions of ENT impairment, as well as adult infertility, to finely characterize the ciliary phenotype. The study also aims to search for new DCP genes and to allow genotype/phenotype correlation studies.
Key facts
- Study ID
- NCT05951478
- Run by
- Institut National de la Santé Et de la Recherche Médicale, France
- People needed
- 300
- Starts
- 2017-05-01
- Expected to finish
- 2027-05-01
- Last updated by the study team
- 2026-02-12
Who can join
Age: any. Sex: any. Healthy volunteers: not accepted.
You may qualify if…
- Patient fulfilling at least one of the following criteria for PCD confirmed diagnosis: Kartagener's syndrome and/or specific anomaly of the ciliary ultrastructure and/or an unambiguous mutation in a PCD gene
- Having at least one annual follow-up visit
- Non-inclusion Criteria:
- Patients with an unconfirmed diagnosis of PCD
- Patients with an evolving concomitant pathology that may interfere with the assessment of PCD-related manifestations
Where it is running
- Hôpital Louis Pradel — Lyon, France (enrolling)
- Hôpital Armand Trousseau — Paris, France (enrolling)
- Hôpital Bichat — Paris, France (enrolling)
- Hôpital Cochin — Paris, France (enrolling)
- Hôpital Necker-Enfants Malades — Paris, France (enrolling)
- Hôpital Tenon — Paris, France (enrolling)
- American Memorial Hospital — Reims, France (enrolling)
- Hospices Civils — Strasbourg, France (enrolling)
- Hôpital des Enfants — Toulouse, France (enrolling)
- Centre Hospitalier Intercommunal de Créteil — Créteil, France (enrolling)
- Centre Hospitalier Intercommunal de Créteil — Créteil, France (enrolling)
- Hôpital Henri Mondor — Créteil, France (enrolling)
- Hôpital Bicêtre — Le Kremlin-Bicêtre, France (enrolling)
- Hôpital Jeanne de Flandre — Lille, France (enrolling)
- Hôpital Femme-Mère-Enfant — Lyon, France (enrolling)
- Hôpital Nord — Marseille, France (enrolling)
- Hôpital Arnaud de Villeneuve — Montpellier, France (enrolling)
- Hôpital Armand Trousseau — Paris, France (enrolling)
- Hôpital de la Timone — Marseille, France
- Hôpital Le Bocage — Dijon, France
- Hôpital Hautepierre — Strasbourg, France
- Hôpital Arnaud de Villeneuve — Montpellier, France
- Hôpital Lenval — Nice, France
- Centre Hospitalier Intercommunal de Créteil — Créteil, France
- Hôpital Larrey — Toulouse, France
Full record on ClinicalTrials.gov
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