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临床试验/NCT01629017
NCT01629017招募中不适用

Longitudinal Evaluation of Recipients of Hematopoietic Stem Cell Transplantation (HSCT)

Stanford University1 个研究点 分布在 1 个国家目标入组 800 人开始时间: 1995年1月1日最近更新:
适应症

试验速览

阶段
不适用
状态
招募中
入组人数
800
试验地点
1
主要终点
Collection of data and tissue samples with the goal of establishing a systematic follow-up care for HSCT recipients and a comprehensive database which can capture the particularities of survivors' clinical status through their life span.

研究概览

简要总结

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.

详细描述

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.

研究设计

研究类型
Observational
观察模型
Case Control
时间视角
Prospective

入排标准

年龄范围
— 至 18 Years(Child, Adult)
性别
All
接受健康志愿者

入选标准

  • 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.

排除标准

  • 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

结局指标

主要结局

Collection of data and tissue samples with the goal of establishing a systematic follow-up care for HSCT recipients and a comprehensive database which can capture the particularities of survivors' clinical status through their life span.

时间窗: This research study is expected to continue as long as we continue to perform clinical trials for children with diseases that involve the bone marrow or are affected by bone marrow production.

次要结局

未报告次要终点

研究者

申办方类型
Other
责任方
Sponsor

研究点 (1)

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