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NCT Number: NCT02442011

Hematology Biobank: In Vitro Study of Blood Disorders

This is a biorepository of blood specimens from subjects with different Hematological disorders.

Recruiting

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Key information

Age range

12 year and older

Sex eligibility

All sexes

Study type

Observational

Primary location

Montefiore Medical Center

The Bronx, New York, 10467, United States

Location status: Recruiting

Location contact

Swati Goel

CONTACT

718-920-4137

About this study

There has been a marked increase in our knowledge of Blood Disorders in the last decade. Much of this knowledge comes from examining blood specimens from patients and subjecting these samples to red cell, plasma, serum or DNA analyses. The study team proposes to set up a Hematology biobank, which will include patient histories, their medical progress and a linked but de-identified bank of blood samples. This will enable researchers to have a large database, which can be used to learn more about these diseases.

The Hematology biobank will use whole blood, red blood cells, plasma, serum and/or DNA. Whole blood specimens, which by definition include the white cells that contain DNA, will be collected and stored in the biobank repository at the Institute for Clinical and Translational Research (ICTR) for future studies.

Blood samples will be obtained from two sources:

  • Leftover/discarded whole blood samples that were obtained for standard of care.
  • Blood samples consisting of 1-5 tubes (3-20 ml of whole blood) from patients with written consent. When possible, these samples will be obtained during routine blood draws performed for a typical visit. It may be necessary to ask patients to specifically donate blood for the study.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Above 12 years of age and referred to the Hematology Division at Montefiore-Einstein
  • Under the care of a Montefiore-Einstein hematologist for a hematologic disorder

Exclusion criteria

  • Do not meet the Inclusion Criteria listed above

Treatment and study plan

Primary outcomes

  1. Biobank

    Time frame: 5 years

    To have specimens available for IRB approved studies

Study contacts

Contact information is provided by the study sponsor or research team.

Swati Goel

CONTACT

[email protected]

7189204137

Sponsors and collaborators

Lead sponsor

Albert Einstein College of Medicine

Other

Collaborators

  • New York Blood Center

Registry information

Important dates

Study start
2014
Primary completion
2030
Study completion
2030
First posted
May 13, 2015
Registry last updated
Jan 6, 2026

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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