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临床试验/NCT03180450
NCT03180450暂停1 期

The Study of Heart Failure With Human Umbilical Cord Mesenchymal Stem Cells (hUC-MSC)

Sclnow Biotechnology Co., Ltd.1 个研究点 分布在 1 个国家目标入组 60 人开始时间: 2025年12月31日最近更新:
适应症
干预措施
相关药物

试验速览

阶段
1 期
状态
暂停
发起方
入组人数
60
试验地点
1
主要终点
Heart color ultrasound evaluation

研究概览

简要总结

The purposes of the study is to evaluate the safety and efficacy of human umbilical cord mesenchymal stem cells (hUC-MSC) in treating heart failure patients

详细描述

This is a randomized, paralleled study. Patients will be divided into two groups of treatment and control. all of them will receive conventional treatment based on specific condition, including digitalis, milrinone, furosemide, beta-blocker blues, Angiotensin-Converting Enzyme Inhibitors (ACEI), angiotension receptor blocker (ARB), and antiplatelet aggregation etc. Treatment group patients will receive hUC-MSC. Follow-up visit will occur on 3 months, 6 months, and 12 months after the cell transfusion. Vital signs, blood routine test, urine routine test, liver function examination, etc, will be placed to evaluate the safety of hUC-MSC treatment. And the change of symptoms to evaluate the efficacy.

研究设计

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

入排标准

年龄范围
18 Years 至 75 Years(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • volunteer to participate in clinical trial, and sign informed consent form
  • with cardiac failure symptoms, including oppression in chest, breathe hard, lower limb edema. And new york heart association class as two to four
  • heart color ultrasound indicate left ventricular ejection fraction (LVEF) < 40%
  • content of serum NT-proBNP > 450pg/ml

排除标准

  • with severe drug allergy history or allergic constitution
  • patients were severe infected
  • with malignant tumor or with high tumor marker
  • with severe cardiorespiratory dysfunction, hematological system disease
  • with severe mental disorder, cognitive impairment
  • with persistent atrial fibrillation, valvular heart disease, dilated cardiomyopathy, hypertrophic cardiomyopathy or restrictive cardiomyopathy patients
  • end-stage renal insufficiency, pregnancy, or breast feeding women
  • bleeding tendency, active gastrointestinal ulcer
  • recent have major surgery, stroke, cancer, hepatic function insufficiency or other life-threatening condition.
  • under other therapy that possibly influence MSC security or efficacy
  • donor: HIV, active hepatitis B/C infection, Syphilitic antibody positive
  • participant/donor: alcoholism, drug addicted, mental disease

研究组 & 干预措施

Treatment group

Experimental

conventional treatment; Allogeneic umbilical cord mesenchymal stem cells (SCLnow 19#) by i.v.

干预措施: Allogeneic umbilical cord mesenchymal stem cells (SCLnow 19#) (Biological)

Treatment group

Experimental

conventional treatment; Allogeneic umbilical cord mesenchymal stem cells (SCLnow 19#) by i.v.

干预措施: conventional treatment (Drug)

Control group

Placebo Comparator

Conventional treatment

干预措施: conventional treatment (Drug)

结局指标

主要结局

Heart color ultrasound evaluation

时间窗: 12 months

Criteria: * Excellent: ejection fraction improve to \> 50%; * Efficient: ejection fraction improved; * Inefficient: ejection fraction same as before treatment; * Exacerbation: ejection fraction declined.

次要结局

  • Single therapy effectiveness evaluation(12 months)

研究者

发起方
Sclnow Biotechnology Co., Ltd.
申办方类型
Industry
责任方
Sponsor

研究点 (1)

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