Tissue Repository: CTCL Collection Protocol
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|ClinicalTrials.gov Identifier: NCT02840747|
Recruitment Status : Recruiting
First Posted : July 21, 2016
Last Update Posted : January 22, 2020
|Condition or disease|
|Lymphoma, T-Cell, Cutaneous Lymphomatoid Papulosis Sézary Syndrome|
CTCL is a heterogeneous group of non-Hodgkin's lymphomas characterized by chronic inflammation and accumulation of malignant T cells in the skin. In order to carry out research to expand the knowledge and develop more effective treatments, tissue samples from CTCL patients with presumed or known disorders are required and tissue samples from control patients will be required to compare the differences between affected and healthy populations.
Scientists will be able to test new ideas and new technologies that are not apparent or available at the present moment from this tissue repository in the future. This type of information will thus be of great advantage to future patients with these diseases.
|Study Type :||Observational|
|Estimated Enrollment :||400 participants|
|Official Title:||A Tissue Repository for the Collection of Samples From Patients With Cutaneous T Cell Lymphoma and Healthy Volunteers|
|Study Start Date :||July 2016|
|Estimated Primary Completion Date :||January 2021|
|Estimated Study Completion Date :||January 2021|
Patients with CTCL
Skin biopsies, blood samples, skin swabs, nasal swabs, cheek epithelium swabs, fecal samples and urine samples may be collected from patients with CTCL (according to World Health Organization-European Organization for Research and Treatment of Cancer (WHO-EORTC) criteria).
Patients with benign dermatoses
Skin biopsies, blood samples, skin swabs, nasal swabs, cheek epithelium swabs, fecal samples and urine samples may be collected from patients with benign dermatoses, including but not limited to conditions such as eczema, psoriasis, and dermatitis.
Skin biopsies, blood samples, skin swabs, nasal swabs, cheek epithelium swabs, fecal samples and urine samples may be collected from healthy volunteers.
- Number of biological specimen collections [ Time Frame: 2 years ]This is a collection protocol to establish a tissue repository for samples from patients with CTCL.
Biospecimen Retention: Samples With DNA
To learn more about this study, you or your doctor may contact the study research staff using the contact information provided by the sponsor.
Please refer to this study by its ClinicalTrials.gov identifier (NCT number): NCT02840747
|Contact: Larisa Geskin, MDfirstname.lastname@example.org|
|Contact: Grace Ulerioemail@example.com|
|United States, New York|
|Columbia University Medical Center||Recruiting|
|New York, New York, United States, 10032|
|Contact: Larisa J Geskin, MD 212-305-5293 firstname.lastname@example.org|
|Contact: Grace Ulerio email@example.com|
|Principal Investigator: Larisa J Geskin, MD|
|Principal Investigator:||Larisa Geskin, MD||Columbia University|