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Biological Sample Collection for Research and Biobanking

Biological Sample Collection for Research and Biobanking

Status
Terminated
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT04270604
Enrollment
1279
Registered
2020-02-17
Start date
2012-02-06
Completion date
2023-11-27
Last updated
2024-08-02

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

ALS, Alzheimer Disease, Cancer, Diabetes Mellitus, Type 1, Huntington Disease, Macular Degeneration, Parkinson Disease

Keywords

stem cell, observational, biobank, disease modeling, genetics

Brief summary

The New York Stem Cell Foundation (NYSCF) Research Institute is performing this research to study different conditions and diseases by using cells from the body (such as skin or blood cells). NYSCF uses these samples to make stem cells and other types of cells, conduct research on the samples, perform genetic testing, and/or store these samples for future use. Through this research, scientists hope to identify future treatments or even cures.

Detailed description

Researchers at NYSCF study diverse diseases, conditions, and traits by creating pluripotent stem cells. These stem cells can become any cell in the human body, including cells that may be difficult, invasive, or even impossible to obtain directly. For example, researchers may create pancreatic insulin-producing cells to learn more about type 1 diabetes, or brain cells to learn more about Parkinson's disease. Additionally, researchers perform genetic testing to learn more about DNA, a material in most cells that contains instructions for the body's development and functions (such as traits like eye color and risk of certain diseases). A piece of DNA that determines the specific role of a cell is called a gene. If the instructions in a gene are abnormal, this can lead to disease. Participation in the study involves: (1) completion of a health questionnaire, (2) providing a skin and/or blood sample from which stem cells may be created, (3) possible collection of a saliva sample for genetic analysis, and (4) possible future follow-up to provide additional information or learn about other research studies. This study is not a clinical trial.

Interventions

OTHERBiological sample collection

Biological sample collection for biobanking and research

Sponsors

New York Stem Cell Foundation Research Institute
Lead SponsorOTHER

Study design

Observational model
OTHER
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
1 Months to 100 Years
Healthy volunteers
Yes

Inclusion criteria

Age * 18 years or older or * Minor with parent/guardian consent Biological Sample Collection * Able and willing to provide: * new samples of blood, skin, and/or saliva specifically for use in this study and/or * excess/leftover samples, cell lines, and/or derivatives that were (or will be) collected for reasons other than this study

Exclusion criteria

* Non-English speaking * Wards of the state * For skin samples collected specifically for this study: history of keloid formation, bleeding disorder, allergy to the anesthetic, or anticoagulation use that precludes sample collection. * For blood samples collected specifically for this study: bleeding disorder, or other medical condition, if the subject's condition increases the risks associated with blood collection. * For saliva samples: inability to produce sufficient saliva or has a condition that precludes sample collection (such as severe trismus). * For prospective samples: refuse to adhere to NYSCF's and/or collaborating site's COVID-19 safety protocols during the COVID-19 pandemic.

Design outcomes

Primary

MeasureTime frameDescription
Establishment of a diverse bank of biological samples, stem cell lines, derivatives, and associated information.BaselineThere are no primary endpoints planned for this biobank; endpoints will be specific to research projects that utilize samples/data contained in the biobank. Projects may investigate the biology, etiology, manifestations, progression, risk factors, genetic underpinnings, and treatment of diseases, conditions, and traits.

Countries

United States

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026