Human Blood Cell Disorders Tissue Bank

NCT ID: NCT00902447

Last Updated: 2024-03-27

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

RECRUITING

Total Enrollment

10000 participants

Study Classification

OBSERVATIONAL

Study Start Date

2009-04-30

Study Completion Date

2035-01-31

Brief Summary

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The Human Blood Cell Disorder Tissue Bank will provide a convenient, comprehensive source of tissue containing populations of human blood cells from patients with various types of lymphoid, myeloid, and erythroid proliferative diseases as well as other associated conditions. The tissue bank will continue to be an invaluable asset for understanding of the biology of multiple blood cell disorders involving several cell types as well as the physiology of normal cellular counterparts affected in these disorders. Internal and external investigators will be able to utilize this tissue to test hypotheses relating to the immunologic, virologic, genetic, and molecular properties of these abnormal cells as well as normal cells from normal unaffected family members or normal aged matched subjects to provide better comparisons.

Detailed Description

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Conditions

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Human Blood Cell Disorders Lymphoid, Myeloid and Erythroid Proliferative Disease

Study Design

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Observational Model Type

CASE_CONTROL

Study Time Perspective

CROSS_SECTIONAL

Study Groups

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Human Blood Cell Disorders

Human Blood Cell Disorders Tissue Bank

No interventions assigned to this group

Eligibility Criteria

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Inclusion Criteria

* Participants or participant's Legally Authorized Representatives (LAR) must be able to understand and render voluntary, written informed consent.
* Patients must be able to contribute the required amount of blood and/or tissue without compromising their well-being or care.
* Participants must be willing to be contacted again for consideration of additional studies in the future, such as a blood draw or another action (e.g., bone marrow aspiration and/or biopsy) that would be done as part of their standard of care.

Exclusion Criteria

* Patients who are known to be anemic, with hemoglobin \<8.0g/dl.
* Patients who are known to be infected with HIV.
Minimum Eligible Age

18 Years

Maximum Eligible Age

100 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

Yes

Sponsors

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Northwell Health

OTHER

Sponsor Role lead

Responsible Party

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Responsibility Role SPONSOR

Principal Investigators

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Nicholas Chiorazzi, M.D.

Role: PRINCIPAL_INVESTIGATOR

Northwell Health

Locations

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The Feinstein Institute for Medical Research

Manhasset, New York, United States

Site Status RECRUITING

Countries

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United States

Central Contacts

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Yasmine Kieso, MSCR

Role: CONTACT

Facility Contacts

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Yasmine Kieso, MSCR

Role: primary

Other Identifiers

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08-202

Identifier Type: -

Identifier Source: org_study_id

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