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临床试验/NCT02179359
NCT02179359终止不适用

MT2014-10C: Allogeneic Hematopoietic Stem Cell Transplant for Patients With High Risk Hemoglobinopathies and Other Red Cell Transfusion Dependent Disorders

Masonic Cancer Center, University of Minnesota1 个研究点 分布在 1 个国家目标入组 38 人开始时间: 2014年9月2日最近更新:
适应症
干预措施
相关药物

试验速览

阶段
不适用
状态
终止
入组人数
38
试验地点
1
主要终点
incidence of graft failure

研究概览

简要总结

This is a study to collect the outcomes of stem cell transplantation for patients with hematologic diseases other than cancer.

研究设计

研究类型
Interventional
分配方式
Non Randomized
干预模型
Single Group
主要目的
Treatment
盲法
None

入排标准

年龄范围
— 至 55 Years(Child, Adult)
性别
All
接受健康志愿者

入选标准

  • Diagnosis of Sickle Cell Disease, Thalassemia, Diamond Blackfan Anemia or other non-malignant hematologic disorders for which a stem cell transplant is indicated
  • Acceptable stem cell source identified
  • Performance status of ≥ 70% (Karnofsky),or ≥ 70 (Lansky play score)
  • Creatinine <2.0 mg/dl for adults or glomerular filtration rate > 50 ml/min for children
  • Bilirubin, Aspartate Aminotransferase, Alkaline phosphatase <5 times the upper limit of institutional normal
  • Absence of decompensated congestive heart failure, or uncontrolled arrhythmia and left ventricular ejection fraction > 40%

排除标准

  • active, uncontrolled infection
  • pregnant or breastfeeding
  • HIV positive

研究组 & 干预措施

Reduced Toxicity Ablative Regimen

Experimental

For use in patients with a matched sibling donor or unrelated UCB donor and DBA patients who are <12 years and/or have mild/moderate iron exposure.

干预措施: Reduced Toxicity Ablative Regimen (Drug)

Reduced Intensity Preparative Regimen

Experimental

For use in patients with unrelated donor bone marrow and for DBA patients who are >12 years and/or have significant iron exposure.

干预措施: Reduced Intensity Preparative Regimen (Drug)

Myeloablative Preparative Regimen

Experimental

For use in patients with a matched sibling donor, unrelated umbilical cord blood and in those with severe thalassemia.

干预措施: Myeloablative Preparative Regimen (Drug)

结局指标

主要结局

incidence of graft failure

时间窗: 42 days

次要结局

  • overall survival(6 months, 1 and 2 years)
  • disease free survival(6 months, 1 and 2 years)

研究者

申办方类型
Other
责任方
Sponsor

研究点 (1)

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