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RecruitingNCT04018118

Natural History of Hypereosinophilia and Hypereosinophilic Syndromes

Study of Clinical Profiles of Patients Followed for Chronic Hypereosinophilia and/or Hypereosinophilic Syndrome by the Creation of a National Cohort

Status
Recruiting
Phase
Study type
Observational
Enrollment
600 (estimated)
Sponsor
University Hospital, Lille · Academic / Other
Sex
All
Age
Healthy volunteers
Not accepted

Summary

Unexplained chronic hypereosinophilia (HE) and hypereosinophilic syndromes (HES) are heterogeneous regarding the organ involvements (heart, lungs, skin, .. or none), the evolutionary profiles, the response to treatments. Underlying mechanisms are largely unknown and may associate genetic predisposing factors (germinal ? somatic?), environmental factors (alimentation, tobacco use, hormones, infections, ..) The COHESion study aims to study all clinical and biological characteristics of HE/HES patients and their evolutionary profiles, with a focus on genetic factors and the mechanisms supporting transitory or persistant chronic HE/HES (in absence of any well identified extrinsic trigger like drugs, parasitosis, ..)

Detailed description

There is currently no data on the natural history of unexplained chronic hypereosinophilia (HE) and hypereosinophilic syndromes (HES). Clinical practice shows that HE/SHE patients can present 4 evolutionary profiles: A. a single flare-up of their disease, with favourable evolution spontaneously or under corticosteroid therapy, without further recurrence B. recurrent flare-ups with a variable free interval of several months to several years, with or without persistent eosinophilia between flare-ups C. a chronic disease requiring the continuation of a substantive treatment D. chronic asymptomatic HE for years: the mechanisms involved in the occurrence of possible organ damage are unknown The primary objective of the study is to describe the frequency of the different clinical manifestations during the diagnostic and follow-up of the hypereosinophilic syndrome (HES). The primary endpoint is the frequency of the different clinical manifestations and/or organs damage related to eosinophilia.

Conditions

Interventions

TypeNameDescription
BIOLOGICALBiological sampleAdditional blood samples for biobanking

Timeline

Start date
2019-05-06
Primary completion
2029-05-06
Completion
2031-05-01
First posted
2019-07-12
Last updated
2026-02-20

Locations

1 site across 1 country: France

Source: ClinicalTrials.gov record NCT04018118. Inclusion in this directory is not an endorsement.

Natural History of Hypereosinophilia and Hypereosinophilic Syndromes (NCT04018118) · Clinical Trials Directory