Actively Recruiting

Age: 18Years +
All Genders
Healthy Volunteers
NCT04330118

Origin and Function of Eosinophilic Polynuclear During DRESS Syndrome

Led by University Hospital, Lille · Updated on 2026-04-22

80

Participants Needed

11

Research Sites

376 weeks

Total Duration

On this page

Sponsors

U

University Hospital, Lille

Lead Sponsor

S

Société de Dermatologie Française

Collaborating Sponsor

AI-Summary

What this Trial Is About

Drug Hypersensitivity Syndrome or DRESS for "Drug Reaction with Eosinophilia and Systemic Symptoms" is a serious drug allergy which can be life-threatening for patients with serious organ damage. The pathophysiology of DRESS is still not fully understood. In particular, no study has focused on the characterization of eosinophils, while paradoxically eosinophilia is one of the diagnostic criteria. Likewise, there is no data about the origin of eosinophils and few data are available concerning immune polarization of T-cells or the involvement of innate lymphoid cells type 2 in the recruitment of eosinophils. Our preliminary data on increase activation markers membrane expression of cutaneous eosinophils suggest that this approach could allow the identification of endotypes in which eosinophils are involved and contribute to organ damages. The correlation between tissue infiltration of eosinophils and their degree of activation would then justify the development of targeted therapeutic strategies in DRESS syndrome (anti-IL-5 therapy?). The aim of the project is: 1) Evaluate the activation status of circulating and cutaneous eosinophils in patients with DRESS compared with drug induced maculopapular exanthema without or with eosinophilia (but do not fulfill DRESS criteria) and healthy subjects; 2) Understand the pathophysiological mechanisms at the origin of this eosinophilia.

CONDITIONS

Official Title

Origin and Function of Eosinophilic Polynuclear During DRESS Syndrome

Who Can Participate

Age: 18Years +
All Genders
Healthy Volunteers

Eligibility Criteria

Eligible

You may qualify if you...

  • Adults diagnosed with DRESS based on rash occurring 24 hours to 2 months after medication, fever over 38°C, organ dysfunction, and hematological anomalies including eosinophilia ≥ 500/mm3 or RegiSCAR Score ≥ 4
  • Adults with drug-induced rash without severe symptoms lasting over 21 days or causing organ damage
  • Adults with drug-induced rash without eosinophilia (blood eosinophils < 500/mm3)
  • Adults with drug-induced rash with eosinophilia (blood eosinophils ≥ 500/mm3)
Not Eligible

You will not qualify if you...

  • Other causes of eosinophilia such as cancer or blood diseases before suspected drug use
  • Use of oral or local corticosteroids, anti-leukotriene therapy in the month before the study
  • Use of anti-IgE, anti-IL-5, or anti-IL4/IL13 therapies in the 6 months before the study
  • Pregnant or breastfeeding women
  • Contraindication to the volume of blood drawn for the study

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Trial Site Locations

Total: 11 locations

1

CH d'Arras

Arras, France

Actively Recruiting

2

CH de Boulogne

Boulogne-sur-Mer, France

Actively Recruiting

3

Assistance Publique - Hôpitaux de Paris - HENRI MONDOR

Créteil, France

Actively Recruiting

4

CH de Douai

Douai, France

Actively Recruiting

5

CH de Dunkerque

Dunkirk, France

Actively Recruiting

6

CH LENS

Lens, France

Actively Recruiting

7

Hop Claude Huriez Chr Lille

Lille, France, 59000

Actively Recruiting

8

Groupe Hospitalier de l'Institut Catholique de Lille

Lille, France

Actively Recruiting

9

CH de Roubaix

Roubaix, France

Actively Recruiting

10

Hôpital FOCH

Suresnes, France

Actively Recruiting

11

CH de Valenciennes

Valenciennes, France

Actively Recruiting

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Research Team

D

Delphine Staumont-Salle, MD,PhD

CONTACT

How is the study designed?

Study Type

OBSERVATIONAL

Masking

N/A

Allocation

N/A

Model

N/A

Primary Purpose

N/A

Number of Arms

4

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