Actively Recruiting
Tissue Repository: CTCL Collection Protocol
Led by Columbia University · Updated on 2025-11-04
400
Participants Needed
1
Research Sites
534 weeks
Total Duration
On this page
AI-Summary
What this Trial Is About
This document is a protocol for a non-interventional human research study in which the investigator hopes to better understand the changes that take place in T cells in Cutaneous T-cell lymphoma (CTCL). The purpose of this study is to establish a protocol for the collection and storage of tissue samples from patients with CTCL for future research studies. Collection and storage of tissue samples from control patients will also be carried out.
CONDITIONS
Official Title
Tissue Repository: CTCL Collection Protocol
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Patients with CTCL or Lymphomatoid Papulosis diagnosed as newly diagnosed, progressive, or relapsed who are starting or changing therapy
- Patients with Sezary Syndrome or stage IV B CTCL defined by specific blood cell criteria
- Ability to understand and sign informed consent
- Age 18 years or older
- Control participants matched for sex and age within 10 years
- Control participants able to sign informed consent
- Controls may have benign inflammatory skin conditions or no skin conditions requiring systemic immunosuppressive, biologic, or chemotherapeutic treatment
You will not qualify if you...
- History of lymphoma other than CTCL, Sezary Syndrome, or Lymphomatoid Papulosis
- Medical illnesses that may affect immune or bowel function as judged by the investigator
- Current viable pregnancy
- Anemia with hemoglobin less than 7.5 g/dl within the past 6 months
- Controls with previous history of CTCL, Sezary Syndrome, Lymphomatoid Papulosis, or any lymphoma
- Controls with previous history of HIV infection
- Controls with anemia with hemoglobin less than 7.5 g/dl within the past 6 months
AI-Screening
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Trial Site Locations
Total: 1 location
1
Columbia University Irving Medical Center
New York, New York, United States, 10032
Actively Recruiting
Research Team
L
Larisa J. Geskin, MD
CONTACT
B
Brigit Lapolla
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
3
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