Adverse Cutaneous Drug Reactions Collection of Clinical Data and Biological Samples

Status: Recruiting
Location: See location...
Study Type: Observational
SUMMARY

Objective: To collect clinical data and cutaneous and biological samples for immunological, biological and genetic studies to improve knowledge about pathophysiology of drug reactions. Method: The following samples will be performed in addition to the routine practice samples: one skin punch biopsy (6mm); 43 mL of blood; blister fluid aspiration; oral and nose mucous membrane and skin eSWABs, stool samples. These samples will be stored in a dedicated biological sampling department (Platform of biological resources).

Conclusion: The implementation of this collection should allow us to conduct pathophysiological studies about drug reactions.

Eligibility
Participation Requirements
Sex: All
Minimum Age: 18
Healthy Volunteers: f
View:

• Patient ≥ 18 y-old

• Severe cutaneous drug reaction (AGEP, DRESS, SJS/TEN, generalized bullous fixed drug eruption), drug-induced IgA bullous dermatosis, maculopapular exanthema, erythema multiforme

• Signed consent

• Social security affiliation

Locations
Other Locations
France
Henri Mondor
RECRUITING
Créteil
Contact Information
Primary
Saskia Oro, MD
saskia.oro@aphp.fr
0149812536
Backup
Laetitia Gregoire
laetitia.gregoire@aphp.fr
0149814164
Time Frame
Start Date: 2018-09-26
Estimated Completion Date: 2028-09-25
Participants
Target number of participants: 500
Sponsors
Leads: Assistance Publique - Hôpitaux de Paris

This content was sourced from clinicaltrials.gov

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