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Adult Pulmonary Langerhans Cell Histiocytosis: a National Registry-based Prospective Cohort Study

A

Assistance Publique - Hôpitaux de Paris

Status

Enrolling

Conditions

Histiocytosis, Langerhans-Cell
Histiocytosis Pulmonary
Histiocytosis

Treatments

Other: Standard of care

Study type

Observational

Funder types

Other

Identifiers

NCT04665674
2014_TAZI

Details and patient eligibility

About

The long-term outcomes of adult patients with pulmonary Langerhans cell histiocytosis (PLCH), particularly survival, is largely unknown. This is the first prospective study in the field evaluating the long-term outcomes of PLCH patients. This french countrywide registry-based study included a large cohort of PLCH patients followed for a sufficiently long period to address risk factors of long-term outcomes of PLCH patients.

Enrollment

500 estimated patients

Sex

All

Ages

18+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Age >= 18 years
  • Diagnosis of PLCH was either histologically confirmed on a biopsy of an involved tissue, or based on the combination of the following criteria: 1) an appropriate clinical picture; 2) a typical nodulo-cystic pattern on lung high-resolution computed tomography (HRCT) and 3) exclusion of alternative diagnoses

Exclusion criteria

Trial design

500 participants in 1 patient group

Pulmonary Langerhans cell histiocytosis (PLCH)
Description:
All patients with newly diagnosed PLCH at adulthood (i.e. 18 years of age or older) referred to the French national reference centre for Histiocytoses
Treatment:
Other: Standard of care

Trial contacts and locations

1

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Central trial contact

matthieu resche-rigon, MD PhD; Abdellatif TAZI, MD PhD

Data sourced from clinicaltrials.gov

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