跳至主要内容
临床试验/JPRN-UMIN000004206
JPRN-UMIN000004206已完成未知

Safety and efficacy of thymoglobulin (ATG) for cord blood transplantation for hematologic malignancies - Safety and efficacy of ATG for CBT for hematologic malignancies

Hematology, Osaka City University, Graduate School of Meicine0 个研究点目标入组 7 人开始时间: 2010年9月14日最近更新:
适应症

试验速览

阶段
未知
状态
已完成
发起方
入组人数
7

研究概览

简要总结

暂无简介。

研究设计

研究类型
Interventional

入排标准

年龄范围
16years-old 至 70years-old(—)
性别
All

入选标准

  • 未提供

排除标准

  • (1)Major organ dysfunction: (a)Ejection fraction: <30% (b)Pulmonary function test: %VC<30%, FEV1.0% <40%, or SaO2 <90% on room air (c)Serum creatinine: >2.0mg/dl (d)Liver function: total bilirubin >2.0mg/dl, AST or ALT >3 x UNL, or patients with chronic active hepatitis or liver cirrhosis (2)Poorly controlled hypertension (3)HIV antibody positivity (4)Uncontrolled active infection (5)Uncontrolled CNS invasion (6)Pregnant, nursing or possibly pregnant woman (7)Patients with severe mental disorder who are likely unable to participate in the study (8)Known hypersensitivity or allergy to any of the drugs in the conditioning regimen of this transplant, or drugs used for GVHD prophylaxis (9)Patients with positive donor-specific HLA antibodies(DSA) (10)Patients with graft failure following allegeneic hematopoietic stem cell transplantation (11)No indication for this study as judged by physician in charge. Note: HBs antigen positivity and HCV antibody positivity is not excluded.

研究者

发起方
Hematology, Osaka City University, Graduate School of Meicine

相似试验