T Cell Response in Hypersensitivity Syndrome
This study has been completed.
Sponsor:
University Hospital, Rouen
Information provided by:
University Hospital, Rouen
ClinicalTrials.gov Identifier:
NCT00213447
First received: September 13, 2005
Last updated: June 11, 2009
Last verified: June 2009
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Purpose
immunological study of the T cell repertoire phenotype and functionality in hypersensitivity syndrome.
| Condition |
|---|
|
Hypersensitivity Syndrome |
| Study Type: | Observational |
| Study Design: | Observational Model: Cohort Time Perspective: Prospective |
| Official Title: | Characterization of T Cell Response in Hypersensitivity Syndrome |
Resource links provided by NLM:
Further study details as provided by University Hospital, Rouen:
Eligibility| Ages Eligible for Study: | 18 Years and older |
| Genders Eligible for Study: | Both |
| Accepts Healthy Volunteers: | No |
| Sampling Method: | Non-Probability Sample |
Study Population
patients with Drug rash with eosinophilia and systemic symptoms
Criteria
Inclusion Criteria:
- age > 18
- cutaneous eruption
- lymph nodes
- hepatitis
- interstitial pneumonia
- nephritis
- cardiopathy
- eosinophilia
- hyperlymphocytosis
Exclusion Criteria:
- age minor to 18
- HIV +
Contacts and Locations
More Information
No publications provided by University Hospital, Rouen
Additional publications automatically indexed to this study by ClinicalTrials.gov Identifier (NCT Number):
| ClinicalTrials.gov Identifier: | NCT00213447 History of Changes |
| Other Study ID Numbers: | 2001/056/HP |
| Study First Received: | September 13, 2005 |
| Last Updated: | June 11, 2009 |
| Health Authority: | France: Ministry of Health |
Additional relevant MeSH terms:
|
Hypersensitivity Immune System Diseases |
ClinicalTrials.gov processed this record on May 16, 2013