Memphis, Tennessee 38105


Purpose:

This protocol allows for ongoing data collection to assess the long-term clinical and psychosocial outcomes of pediatric patients who have received a hematopoietic stem cell transplant at St. Jude Children's Research Hospital.


Study summary:

The purpose of this protocol is to provide ongoing data collection and review of long-term outcome and late effects in a large cohort of St. Jude Children's Research Hospital autologous and allogeneic hematopoietic stem cell recipients. Central coordination of clinical and psychosocial late effects monitoring and reporting can facilitate timely communication about life-threatening or unanticipated clinical outcomes as well as significant psychological, social and behavioral sequelae effects on the recipient and their family members. The resultant data may enable researchers in their development of current clinical and psychosocial studies, as well as monitoring predisposed survivors who may benefit from preventive or corrective interventions. Physicians and researchers may be able to learn how to identify these problems earlier, to take better care of these problems, or to implement preventive measures for future transplant recipients


Criteria:

Inclusion Criteria: - St. Jude patients actively monitored in the BMT-AFU clinic after receiving HSC transplant for a malignant or non-malignant condition. - St. Jude alumnus who has received a hematopoietic stem cell transplant for a malignant or non-malignant condition and is monitored by the Tumor Registry


NCT ID:

NCT00674882


Primary Contact:

Principal Investigator
Brandon Triplett, MD
St. Jude Children's Research Hospital

Brandon Triplett, MD
Phone: 866-278-5833
Email: referralinfo@stjude.org


Backup Contact:

N/A


Location Contact:

Memphis, Tennessee 38105
United States

Brandon Triplett, MD
Phone: 866-278-5833
Email: referralinfo@stjude.org

Site Status: Recruiting


Data Source: ClinicalTrials.gov

Date Processed: March 16, 2018

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