Medical Information Only. Always consult your healthcare provider before enrolling in any clinical trial.
A Registry for People With T-cell Lymphoma
NCT05978141 · View on ClinicalTrials.gov ↗
Study Summary
The purpose of this registry study is to create a database-a collection of information-for better understanding T-cell lymphoma. Researchers will use the information from this database to learn more about how to improve outcomes for people with T-cell lymphoma.
Conditions Studied
Interventions
- OTHER Optional Blood Sample and Nail Sample
Study Locations (20)
California
- City of Hope Cancer Center (Data collection only) — Duarte
- UNIVERSITY OF CALIFORNIA SAN DIEGO (Data collection only) — San Diego
- University of California San Francisco (Data collection only) — San Francisco
- Stanford University Medical Center (Data collection only) — Stanford
New York
- Memorial Sloan Kettering Cancer Center @ Suffolk-Commack (All protocol activities) — Commack
- Memorial Sloan Kettering Westchester (All protocol activities) — Harrison
- Weill Cornell Medical Center (Data Collection Only) — New York
Florida
- University of Miami (Data Collection Only) — Miami
- Moffitt Cancer Center (Data Collection Only) — Tampa
Massachusetts
- Massachusetts General Hospital (Data Collection Only) — Boston
- Dana Farber Cancer Institute (Data Collection Only) — Boston
New Jersey
- Memorial Sloan Kettering at Basking Ridge (All protocol activities) — Basking Ridge
- Memorial Sloan Kettering Monmouth (All protocol activities) — Middletown
Colorado
- University of Colorado (Data Collection Only) — Aurora
Connecticut
- Yale University (Data Collection Only) — New Haven
Georgia
- Emory University (Data Collection Only) — Atlanta
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 1,000 participants |
| Start Date | 2023-07-27 |
| Est. Completion | 2030-07-27 |
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Full Details on ClinicalTrials.gov ↗What the Registry Record Tells You About NCT05978141
The ClinicalTrials.gov registry entry for NCT05978141 describes a study currently listed as recruiting. It is categorized as an unspecified phase, which is the standard way researchers label where a study sits along the investigational pathway from early safety work through later efficacy and post-marketing evaluation. The registered enrollment target is 1,000 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is Memorial Sloan Kettering Cancer Center, which has 2,280 total studies on file at ClinicalTrials.gov, and sponsors are the parties responsible for study design, oversight, and regulatory filings.
The record links to 10 conditions, with T-cell Lymphoma appearing as the primary indexed condition, and to 1 intervention — of which Optional Blood Sample and Nail Sample is the first listed. Interventions can include drugs, devices, procedures, behavioral programs, or observational arms, and each is tracked as a separate registry field so that downstream queries can filter accurately. When a trial lists multiple interventions, it usually reflects a multi-arm design or a comparison protocol rather than a single treatment being tested in isolation. The brief summary published in the registry is the clearest source of protocol intent and should be read before drawing conclusions from any sidebar tags.
Geographic footprint matters for practical reasons: NCT05978141 reports 20 study locations spanning 12 distinct geographic areas — top geographies include California, New York, Florida. A larger site network tends to correlate with broader recruitment capacity, but it does not imply anything about study quality, and site-level enrollment status can diverge from the overall registry status shown above. Every data point on this page comes from the public ClinicalTrials.gov dataset and is reproduced here for reference only; it is not a medical recommendation, an endorsement of the sponsor, or an invitation to enroll. Verify current status, eligibility criteria, and contact details directly at ClinicalTrials.gov, and discuss any participation decision with your own healthcare provider.
Frequently Asked Questions
What is clinical trial NCT05978141 about?
NCT05978141 is a clinical study titled "A Registry for People With T-cell Lymphoma". The purpose of this registry study is to create a database-a collection of information-for better understanding T-cell lymphoma. Researchers will use the information from this database to learn more about how to improve outcomes for people with T-cell lymphoma.
What is the current status of trial NCT05978141?
This trial is currently recruiting. The enrollment target is 1,000 participants. The study started on 2023-07-27. Estimated completion is 2030-07-27.
What conditions does trial NCT05978141 study?
This clinical trial studies the following conditions: T-cell Lymphoma, T-cell Prolymphocytic Leukemia, NK-Cell Lymphoma, T-cell Large Granular Lymphocytic Leukemia, Hydroa Vacciniforme-Like Lymphoproliferative Disorder. These conditions were identified from the trial registry and reflect the primary focus areas of the research.
What interventions are being tested in trial NCT05978141?
The interventions under investigation include: Optional Blood Sample and Nail Sample (OTHER). Each intervention is being evaluated for safety and efficacy as part of this clinical study.
Who is sponsoring clinical trial NCT05978141?
This trial is sponsored by Memorial Sloan Kettering Cancer Center, which has 2,280 total clinical trials registered on ClinicalTrials.gov. The sponsor is responsible for the study's design, funding, and regulatory compliance.
Where is trial NCT05978141 being conducted?
This trial has 20 study locations across California, Colorado, Connecticut, Florida, Georgia. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.
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