Silent Infarct Transfusion Trial (SITT)

Study ID
Study00000074

Cancer Related
No

Healthy Volunteers
No

Study Sites

  • Children's Medical Center-Dallas

Contact
Michael Henson
214-456-6525
michael.henson@childrens.com

Principal Investigator
Timothy McCavit

Summary

Eligible subjects who have sickle cell disease will undergo a screening MRI of the brain and transcranial Doppler ultrasonography (TCD). Those who have
* silent infarcts
* on MRI and no increased risk of overt stroke (determined by TCD) may then be randomized to receive either red blood cell transfusions (preferably by erythrocytapheresis, alternatively by simple transfusion) or observation for 3 years. The primary outcome, the occurrence of new silent or overt stroke, will be determined by serial physical examinations and MRI of the brain. Neuropsychological testing will be completed on all subjects to assess their learning, thinking, and memory abilities over time. Subjects and their families will undergo multiple education sessions in which the alternatives to and the implications of the study will be presented and discussed. Subjects will also participate in genetic studies to determine associations between genetic polymorphisms and stroke (or absence of stroke). Blood (plasma) will also be obtained at certain visits on some of the participants to study proteins and other factors associated with strokes or sickle cell severity.

Participant Eligibility

2.31 Inclusion Criteria for Screening
1. Patient must have sickle cell anemia (hemoglobin SS) or sickle β[Degrees] thalassemia (hemoglobin Sβ[Degrees]) as confirmed at the local institution by hemoglobin analysis after six months of age.
2. Patient must be 5 through 14 years of age (i.e., must have attained their 5th, but not their 15th birthday when the screening consent is signed).
3. Informed consent with assent in accordance with the institutional policies (institutional IRB approval) and Federal guidelines (approved by the United States Department of Health and Human Services) must be signed by the patient's legally authorized guardian acknowledging written consent to join the study. When suitable, patients will be requested to give their assent to join the study.