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Clinical Trials/NCT01174615
NCT01174615
Recruiting
Not Applicable

Collection of Blood and/or Bone Marrow for Investigation and Characterization of Normal and Abnormal Cell Growth in Patients With Malignancy or Hematologic Disorders

University of Massachusetts, Worcester1 site in 1 country1,000 target enrollmentSeptember 2009
ConditionsLeukemia

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Leukemia
Sponsor
University of Massachusetts, Worcester
Enrollment
1000
Locations
1
Primary Endpoint
The study is designed to collect blood and bone marrow from patients with various hematological diseases.
Status
Recruiting
Last Updated
2 years ago

Overview

Brief Summary

The collection of Blood and/or Bone Marrow from patients with blood disorders, blood cell malignancies and associated conditions will serve as a convenient and comprehensive source of tissue to give us further information about the differences between normal blood cells and blood cells of affected individuals. This will be an invaluable asset for understanding the biology of blood disorders. The collected samples will be used by investigators for studies including immunology, molecular biology and genetics to name a few.

Registry
clinicaltrials.gov
Start Date
September 2009
End Date
December 2100
Last Updated
2 years ago
Study Type
Observational
Sex
All

Investigators

Sponsor
University of Massachusetts, Worcester
Responsible Party
Principal Investigator
Principal Investigator

Jan Cerny

Principal Investigator

University of Massachusetts, Worcester

Eligibility Criteria

Inclusion Criteria

  • Selected patients over the age of 18 with hematologic malignancies or other blood disorders (leukemia, myeloproliferative disorders, lymphoma, other malignancies involving the bone marrow or patients with unexplained alterations in their complete blood count).
  • Patients who are scheduled to undergo a bone marrow aspirate and/or phlebotomy for other clinical indications will be asked to participate. They will be asked to donate an additional small aliquot of bone marrow and/or blood during the course of their already scheduled bone marrow aspiration or phlebotomy.

Exclusion Criteria

  • Patients with pre-existing medical conditions that might be exacerbated by the procedure of obtaining bone marrow or blood
  • Patients who are allergic to Lidocaine, which is used as a local anesthetic, and who cannot receive a suitable substitute anesthetic.
  • Patients who have a bleeding diathesis which might pose a problem with marrow aspiration.
  • Patients unable to give informed consent.
  • Pregnant patients

Outcomes

Primary Outcomes

The study is designed to collect blood and bone marrow from patients with various hematological diseases.

Time Frame: On average, indefinite, or until death of participant

The study is designed to collect blood and bone marrow from patients with various hematological diseases. The samples will be used for various research studies for better understanding of biology of various blood disorders including hematological malignancies. Relevant clinical and laboratory features and subsequent changes will be noted for correlation with these studies. The tissue/cells will be additionally banked and/or used for other investigations in the future.

Secondary Outcomes

  • Collection of Blood and/or Bone Marrow for Investigation and Characterization of Normal and Abnormal Cell Growth in Patients With Malignancy or Hematologic Disorders(On average, indefinite, or until death of participant)

Study Sites (1)

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