Clinical Trials Logo

Clinical Trial Details — Status: Recruiting

Administrative data

NCT number NCT00902447
Other study ID # 08-202
Secondary ID
Status Recruiting
Phase
First received
Last updated
Start date April 2009
Est. completion date January 2035

Study information

Verified date March 2024
Source Northwell Health
Contact Yasmine Kieso, MSCR
Email ykieso@northwell.edu
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

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.


Recruitment information / eligibility

Status Recruiting
Enrollment 10000
Est. completion date January 2035
Est. primary completion date January 2030
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group 18 Years to 100 Years
Eligibility 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.

Study Design


Related Conditions & MeSH terms


Locations

Country Name City State
United States The Feinstein Institute for Medical Research Manhasset New York

Sponsors (1)

Lead Sponsor Collaborator
Northwell Health

Country where clinical trial is conducted

United States, 

Outcome

Type Measure Description Time frame Safety issue
Primary Accumulate tissue from patients with various blood disorders, including but not restricted to lymphoproliferative, myeloproliferative, and erythroproliferative conditions. Indefinite
Secondary Develop a database of at least 10,000 subjects who have donated samples for research as well as DNA banking, and who are willing to be contacted again for consideration of additional studies in the future. Indefinite