EUCTR2006-004101-26-BE进行中(未招募)不适用
Mesenchymal stem cell infusion as prevention for graft rejection and graft-versus-host disease after allogeneic hematopoietic cell transplantation with nonmyeloablative conditioning: a pilot study - NA
CHU Sart-Tilman0 个研究点开始时间: 2006年9月28日最近更新:
适应症
试验速览
- 阶段
- 不适用
- 状态
- 进行中(未招募)
- 发起方
研究概览
简要总结
暂无简介。
研究设计
- 研究类型
- Interventional clinical trial of medicinal product
入排标准
- 性别
- All
入选标准
- •1. Hematological malignancies confirmed histologically and not rapidly progressing.
- •2. Theoretical indication for a standard allo-transplant, but not feasible because:
- •Age > 55 yrs; Unacceptable end organ performance; Patient’s refusal. OR
- •Indication for a standard auto-transplant: perform mini-allotransplantation 2-6 months after standard autotransplant.
- •3. Male or female; fertile female patients must use a reliable contraception method;
- •4 Age 5 Informed consent given by patient or his/her guardian if of minor age.
- •6 HLA-compatibility with HSC or cord blood donor as described in the protocol
- •1 Related to the recipient (sibling, parent or child) or unrelated;
- •2 Fulfills generally accepted criteria for allogeneic PBSC donation;
- •3 Informed consent given by donor or his/her guardian if of minor age, as per donor center standard procedures.
- •Are the trial subjects under 18? yes
- •Number of subjects for this age range:
- •F.1.2 Adults (18-64 years) yes
- •F.1.2.1 Number of subjects for this age range
- •F.1.3 Elderly (>=65 years) yes
- •F.1.3.1 Number of subjects for this age range
排除标准
- •1 Any condition not fulfilling inclusion criteria;
- •2 HIV positive;
- •3 Terminal organ failure, except for renal failure (dialysis acceptable);
- •4 Uncontrolled infection, arrhythmia or hypertension;
- •5 Previous radiation therapy precluding the use of 2 Gy TBI;
- •6 HLA-identical donor.
- •1 Any condition not fulfilling inclusion criteria;
- •2 HIV positive;
- •3 Unable to undergo leukapheresis because of poor vein access or other reasons.
研究者
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