Cell Therapy With Mesenchymal Stem Cell in Ischemic Limb Disease
试验速览
- 阶段
- 1 期
- 状态
- 已完成
- 入组人数
- 18
- 试验地点
- 1
- 主要终点
- Adverse events
研究概览
简要总结
Bone marrow MSCs will be isolated from allogenic donors, expanded under hypoxic conditions using medium containing no serum or animal-derived reagents, and applies for Phase Ⅰ/Ⅱ study in treating 18 recipients with ischemic limb diseases.
详细描述
Ischemic limb disease remains one of the major causes of morbidity and mortality in the industrialized world despite the development of several new therapeutic modalities. Based on experimental data demonstrating that infusion or injection of stem/progenitor cells enhances blood flow in models of cardiovascular diseases, clinical trials were initiated in 2001 to treat patients with critical limb ischemia or cardiac ischemia with circulating blood or bone marrow-derived cells. Despite all promises, pending uncertainties and practical limitations attenuate the therapeutic use of stem/progenitor cells for ischemic limb disease. The main theme and method in the current program project, based on expertise, track record, and preliminary results of PI's laboratory, is to focus on clinical studies of using allogenic mesenchymal stem cells (MSCs), expanded under hypoxic conditions (1% O2), in treating ischemic limbs. This project is an integrated and coordinated effort aimed to overcome the regulation of cell product, and the barriers of preclinical and clinical studies. For the purposes, we have specially set up the core laboratory for stem/progenitor cells production and quality control in Cell Therapy Clean Room on the 9th floor of Medical Science Technology Building in Taipei Veterans General Hospital. We have also completed the preclinical studies in using allogenic hypoxic mouse MSCs in treating limb ischemia. In the current project, bone marrow MSCs will be isolated from allogenic donors, expanded under hypoxic conditions using medium containing no serum or animal-derived reagents, and applies for Phase Ⅰ/Ⅱ study in treating 18 recipients with ischemic limb diseases in three years.
研究设计
- 研究类型
- Interventional
- 分配方式
- Randomized
- 干预模型
- Single Group
- 主要目的
- Treatment
- 盲法
- Double (Participant, Investigator)
入排标准
- 年龄范围
- 20 Years 至 80 Years(Adult, Older Adult)
- 性别
- All
- 接受健康志愿者
- 否
入选标准
- •Fontaine stage > II, total walking distance < 100 m, stair < 1 floor, or ulcer / necrosis
- •Established critical limb ischemia, clinically and hemodynamically confirmed as per Rutherford- Ⅱ-4, Ⅲ-5, or Ⅲ-6; Patients having Infra-inguinal arterial occlusive disease with rest pain or ischemic ulcer/necrosis, who are not eligible for or have failed traditional revascularization treatment
- •Ankle Brachial Pressure Index (ABPI) ≤ 0.8,ankle pressure ≤ 70 mm Hg, or TcPO2 ≤ 70 mmHg in the foot
- •No response to medication (aspirin and cilostazol)
- •Normal liver and renal function
- •On regular medication for hypertension if any
排除标准
- •The above mentioned patients combined with infection or systemic septicemia. (ps, patients with poor control of diabetes, hypertension and hyperlipidemia will also be excluded
- •Patient with Immunocompromised or immunosuppressed
- •Type I Diabetes
- •Patients having stroke or myocardial infarction within last 3 months
- •Hb% < 10 gm%, Serum Creatinine ≥ 2mg%, Serum Total Bilirubin ≥2mg%, HbA1c > 8%
研究组 & 干预措施
Low Dose Allogenic MSC
Low dose allogenic mesenchymal stem cells with IM injection
干预措施: Allogenic MSC (Drug)
High Dose Allogenic MSC
High dose allogenic mesenchymal stem cells with IM injection
干预措施: Allogenic MSC (Drug)
Placebo
normal saline with Intramuscular injection
干预措施: Normal saline (Drug)
结局指标
主要结局
Adverse events
时间窗: 6 months
Number of adverse events reported
次要结局
- Efficacy-The Wong Baker FACES® pain rating scale(6 months)
- Efficacy-Transcutaneous oxygen pressure(TcPO2)(6 months)
- Efficacy-walking distance (TWD)(6 months)
- Efficacy-Ankle Brachial Pressure Index (ABPI)(6 months)
