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By physician referral or invitation only

GRNDaD

To have a well phenotyped cohort of people with sickle cell disease in order to examine risk factors for end organ disease through the creation of a multi-site registry and to develop a repository for the long-term storage of patient samples (whole blood, peripheral blood, serum) along with corresponding demographic and clinical information to allow for clinical and laboratory correlations.

Age & Gender

  • 0 years ~ 0 years
  • Male, Female, Gender Inclusive

Contact the Team

Location

Thank you for your interest, but this study is recruiting by invitation only.

Additional Study Information

Principal Investigator

Jane Little
Medicine-Hematology

Study Type

Clinical or Medical
Registry

Study Topics

Blood Conditions
Minority Health
Pain

IRB Number

19-0922

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