Long Term Effects On Recipients of Hematopoietic Stem Cell Transplantation



Status:Recruiting
Conditions:Hematology
Therapuetic Areas:Hematology
Healthy:No
Age Range:Any - 18
Updated:2/13/2019
Start Date:January 1995
End Date:January 2099

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This project allows for the systematic collection and analysis of long-term follow-up
clinical parameters in children who have received a stem cell transplant. The data collected
will assist in determining appropriate intervention and treatment plans for patients enrolled
on this study. In addition, future patients may benefit by having the ability to anticipate
problems and develop methods of prevention or early intervention.

Primary Objective: Implement long-term follow-up guidelines for children, adolescents and
young adults who are survivors of HSCT while establishing a database which captures the
survivor's lifetime care.

Secondary Objectives:

- Collect evidence-based data through a structured framework of periodic physical
examination, laboratory and medical tests to monitor late effects in our HSCT survivors.

- Establish standards of care for late effects of therapy post HSCT for malignant and
non-malignant diagnoses.

- Provide early identification and intervention towards recognized problems, as well as
consistent education to foster a healthy lifestyle to all survivors.

- Collect blood and tissue samples to study immune reconstitution of all immune cell types
and learn more about immune reconstitution and its affect on post-HSCT complications and
disease free survival.

Inclusion Criteria:

- Participant is scheduled to receive OR has received a hematopoietic stem cell
transplant (HSCT) for any condition.

- Participant may have had a HSCT in another institution than Lucile Packard Children's
Hospital (LPCH) yet has transferred follow-up long-term care to our institution and is
being seen through the late-effects clinic from the Pediatric HSCT program.

- Participant AND/OR parent/legally authorized representative is able to provide written
informed consent and assent (as applicable) for participation.

Exclusion Criteria:

- Participant has relapsed from a malignant diagnosis post HSCT and is not being
worked-up for a new HSCT.

- Participant or patient's authorized guardian is unable to provide consent and assent
We found this trial at
1
site
291 Campus Dr
Stanford, California 94305
(650) 725-3900
Principal Investigator: Rajni Agarwal-Hashmi
Phone: 650-724-9179
Stanford University School of Medicine Vast in both its physical scale and its impact on...
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Stanford, CA
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