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Blood, Urine, and Tissue Collection for Cutaneous Lymphoma, Eczema, and Atopic Dermatitis Research

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University of Pittsburgh

Status

Enrolling

Conditions

Atopic Dermatitis
Cutaneous T-cell Lymphoma
Mycosis Fungoides
Sezary Syndrome
Eczema

Treatments

Other: Blood draw, skin biopsy or urine collection

Study type

Observational

Funder types

Other

Identifiers

NCT00177268
STUDY19010322

Details and patient eligibility

About

This is a tissue, urine, and blood banking protocol for cutaneous t-cell lymphoma (CTCL), eczema, and atopic dermatitis patients for current and future research.

Full description

The purpose of this study is to provide a central mechanism for monitoring access to peripheral blood, urine, and skin specimens obtained from CTCL, eczema, and atopic dermatitis patients to monitor:

  • immunologic assays/flow cytometry
  • tumor progression/regression
  • genomic studies
  • proteomic studies
  • others germane to the advancement of CTCL treatment

Enrollment

200 estimated patients

Sex

All

Ages

18+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • 18 or older
  • able and willing to provide informed consent
  • diagnosed with CTCL
  • diagnosed with either atopic dermatitis or eczema

Exclusion criteria

  • Lack of CTCL, atopic dermatitis, or eczema diagnosis in medical record

Trial design

200 participants in 1 patient group

CTCL, atopic dermatitis, eczema
Description:
Those subjects with cutaneous t-cell lymphoma and Sezary syndrome, atopic dermatitis, or eczema may participate as appropriate with the potential for blood, tissue or urine sampling.
Treatment:
Other: Blood draw, skin biopsy or urine collection

Trial contacts and locations

1

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Central trial contact

Charity L Ruhl, LPN

Data sourced from clinicaltrials.gov

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