Stanford, California 94305

  • Blood and Marrow Transplant (BMT)

Purpose:

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.


Study summary:

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.


Criteria:

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


NCT ID:

NCT01629017


Primary Contact:

Principal Investigator
Ami Shah
Stanford University


Backup Contact:

N/A


Location Contact:

Stanford, California 94305
United States

Leigh Shinn
Phone: 650-724-9179
Email: leighs@stanford.edu

Site Status: Recruiting


Data Source: ClinicalTrials.gov

Date Processed: September 27, 2021

Modifications to this listing: Only selected fields are shown, please use the link below to view all information about this clinical trial.


Click to view Full Listing

If you would like to be contacted by the clinical trial representative please fill out the form below.