Allogeneic Mesenchymal Stem Cells for the Critical Limb Ischemia Therapy
The clinical trial aims to study the safety and efficacy of adult allogeneic mesenchymal stem cells for the treatment of critical limb ischemia.
研究概览
研究类型
介入性
注册 (预期的)
40
阶段
- 阶段2
- 阶段1
联系人和位置
本节提供了进行研究的人员的详细联系信息,以及有关进行该研究的地点的信息。
学习地点
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Moscow、俄罗斯联邦
- 招聘中
- Federal Research Clinical Center of Federal Medical & Biological Agency
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接触:
- Mikhail A Konoplyannikov, PhD
- 电话号码:+79154027268
- 邮箱:mkonopl@mail.ru
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参与标准
研究人员寻找符合特定描述的人,称为资格标准。这些标准的一些例子是一个人的一般健康状况或先前的治疗。
资格标准
适合学习的年龄
18年 至 80年 (成人、年长者)
接受健康志愿者
不
有资格学习的性别
全部
描述
Inclusion Criteria:
- Males or females in the age group of 18-80 yrs of Caucasian origin.
- Peripheral artery disease (PAD) against the background of atherosclerosis and diabetes mellitus (DM)
- Critical lower limb ischemia (stages 3-4 by Fontaine-Pokrovsky or stages 4-6 by Rutherford)
- Patients with remaining symptoms of critical limb ischemia (CLI) in spite of the performed surgical (endovascular or open) treatment and continuing conservative therapy
- Patients with absent emergency indications to major amputation
- Patients planned for the reconstructive surgery with a questionable remote outcome due to compromised blood outflow
- Ankle Brachial Pressure Index (ABPI) ≤ 0.5 or ankle pressure ≤ 70 mm Hg
- Patients, if having associated Type II Diabetes, should be on medication and well controlled (HbA1c ≤ 8.5 %)
- On regular medication for hypertension if needed
- Normal liver and renal function (or having clinically insignificant deviations, according to the treating physician's opinion)
- Patients who are able to understand the requirements of the study, and willing to provide voluntary written informed consent, abide by the study requirements, and agree to return for required follow-up visits
Exclusion Criteria:
- Humid gangrene or acute/chronic infection of lower limb.
- Dry gangrene with extensive foot lesion (> 1\2).
- Acute arterial failure.
- Life-threatening conditions and predicted life expectancy of < 6 months.
- Presence of neoplasm or bone marrow disease
- Signs of active or chronic, including latent, haemorrhage
- Any acute or chronic infectious disease
- Renal failure determined as twofold or higher elevation of serum creatinine as compared to the upper normal limit
- Hepatic failure determined as the bilirubin, alanine aminotransferase (ALT) or aspartate aminotransferase (AST) levels elevated by two and more times over the upper normal limits
- Thrombocytopenia (platelet counts < 50,000 /µl), leukocytopenia (WBC < 4,000/µl), immunosuppressive therapy
- Pronounced neurological deficit
- Patients with gait disturbance for reasons other than CLI
- Patients not suitable for cell therapy, by the treating physician's opinion
- CLI patients requiring amputation at the proximal to the trans-metatarsal level
- Patients with Type I diabetes
- Patients having respiratory complications/left ventricular ejection fraction < 25%
- Stroke or myocardial infarction within last 3 months
- Patients who are contraindicated for X-ray angiography
- History of severe alcohol or drug abuse within 3 months of screening
- Pregnant and lactating women.
- Patients tested positive for HIV 1, hepatitis C virus (HCV), hepatitis B virus (HBV)
- Unsigned informed consent
学习计划
本节提供研究计划的详细信息,包括研究的设计方式和研究的衡量标准。
研究是如何设计的?
设计细节
- 主要用途:治疗
- 分配:非随机化
- 介入模型:并行分配
- 屏蔽:单身的
武器和干预
参与者组/臂 |
干预/治疗 |
|---|---|
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实验性的:Mesenchymal stem cells
Mesenchymal stem cells, Intramuscular injection
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Intramuscular injection
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安慰剂比较:Normal saline
Normal saline, Intramuscular injection
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Intramuscular injection
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研究衡量的是什么?
主要结果指标
结果测量 |
措施说明 |
大体时间 |
|---|---|---|
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Adverse events
大体时间:24 months
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Number of adverse events reported
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24 months
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Amputation-free survival
大体时间:24 months
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Number of survived patients
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24 months
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次要结果测量
结果测量 |
措施说明 |
大体时间 |
|---|---|---|
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Limb salvage from major amputation
大体时间:3, 6, 12, 24 months
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Number of patients who avoided amputation
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3, 6, 12, 24 months
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Relief of the rest pain
大体时间:Immediate, 3, 6, 12, 24 months
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Rest pain will be measured using the rest pain scale
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Immediate, 3, 6, 12, 24 months
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Improvement in healing trophic disorders
大体时间:Immediate, 3, 6, 12, 24 months
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Assessment of the severity of trophic ulcers
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Immediate, 3, 6, 12, 24 months
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Improvement in perfusion by the ankle-brachial index
大体时间:Immediate, 3, 6, 12, 24 months
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Measurements of the ankle-brachial index
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Immediate, 3, 6, 12, 24 months
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Improvement in perfusion by radioisotope scintigraphy
大体时间:Immediate, 3, 6, 12, 24 months
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Radioisotope scintigraphy study
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Immediate, 3, 6, 12, 24 months
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Improvement in total walking distance (TWD) using a standard treadmill test
大体时间:Immediate, 3, 6, 12, 24 months
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Standard treadmill test
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Immediate, 3, 6, 12, 24 months
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合作者和调查者
在这里您可以找到参与这项研究的人员和组织。
调查人员
- 研究主任:Vladimir P Baklaushev, MD, PhD、Deputy Director
- 首席研究员:Pavel Yu Orekhov, MD, PhD、Vascular Surgeon
研究记录日期
这些日期跟踪向 ClinicalTrials.gov 提交研究记录和摘要结果的进度。研究记录和报告的结果由国家医学图书馆 (NLM) 审查,以确保它们在发布到公共网站之前符合特定的质量控制标准。
研究主要日期
学习开始 (实际的)
2013年10月1日
初级完成 (预期的)
2018年8月1日
研究完成 (预期的)
2018年11月1日
研究注册日期
首次提交
2017年7月20日
首先提交符合 QC 标准的
2017年8月1日
首次发布 (实际的)
2017年8月4日
研究记录更新
最后更新发布 (实际的)
2017年8月4日
上次提交的符合 QC 标准的更新
2017年8月1日
最后验证
2017年8月1日
更多信息
此信息直接从 clinicaltrials.gov 网站检索,没有任何更改。如果您有任何更改、删除或更新研究详细信息的请求,请联系 register@clinicaltrials.gov. clinicaltrials.gov 上实施更改,我们的网站上也会自动更新.
Mesenchymal stem cells的临床试验
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Universidad de la SabanaFundación Neumologica Colombiana; Stem Medicina Regenerativa; Innocell SAS可用的
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The First Affiliated Hospital of Soochow UniversityFundamenta Therapeutics, Ltd.招聘中
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Oregon Research Behavioral Intervention Strategies...National Institute on Minority Health and Health Disparities (NIMHD)完全的
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Ohio State UniversityUniversity of Chicago; National Institutes of Health (NIH); Resilient Games Studio终止