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临床试验/NCT02941419
NCT02941419已完成1 期

Safety and Efficacy of Platelet Lysate for Therapeutic Angiogenesis in Patients With Peripheral Arterial Disease

University of Jordan0 个研究点目标入组 10 人开始时间: 2013年3月5日最近更新:
适应症
干预措施

试验速览

阶段
1 期
状态
已完成
入组人数
10
主要终点
Assessment the safety of platelet lysate injection

研究概览

简要总结

Induction of autologous angiogenesis in patients with critical limb ischemia using platelet lysate.

详细描述

Ten male and female patients diagnosed with Peripheral artery disease (PAD), will be recruited. This diagnosis will be based on medical history, physical examinations, laboratory tests, and specific diagnostic tests. Patients qualified for this study, are patients with distal extremity ischemia indicated by claudication and rest pain present for a minimum of 4 weeks without evidence of improvement in response to conventional drug therapy; showed angiographic evidence of PAD in the affected limb; and were not candidates for surgical revascularization. Platelet lysate will be injected intramuscularly at different sites of the gastrocnemius muscle. The purpose of this study is to evaluate the safety and efficacy of platelet lysate injections into ischematic limbs of patients with PAD.

研究设计

研究类型
Interventional
分配方式
Na
干预模型
Single Group
主要目的
Treatment
盲法
None

入排标准

年龄范围
18 Years 至 70 Years(Adult, Older Adult)
性别
All
接受健康志愿者
否

入选标准

  • •Competent and willing to give informed consent, and to be available for all baseline treatment and follow up examinations required by the protocol.
  • •Gender: Male or female.
  • •Established Peripheral arterial disease, clinically and hemodynamically confirmed as per Rutherford 3, 4 and
  • •History of intermittent claudication for > eight weeks.
  • •Limited exercise due to moderate to severe claudication.
  • •Resting ankle brachial index (ABI) < 0.85, toe pressure ≤ 60 mm Hg, Toe brachial index (TBI) <0.6, or Trans-cutaneous oxygen pressure (TcPO2) ≤ 60 mmHg in the foot.
  • •Not eligible for surgical or radiological revascularization.
  • •In case of diabetic patients, he/she should be on medication and fairly controlled (HbA1c <10%).
  • •Normal liver enzymes, serum creatinine < 1.4
  • •Normal platelet count.
  • •On regular medication for hypertension if any.
  • •No evidence of malignancy
  • •Low Questionnaire scores.
  • •Body mass index <30.

排除标准

  • •Women with child bearing potential, pregnant and lactating women.
  • •Rheumatoid Arthritis.
  • •History of neoplasm or malignancy in the past 10 years.
  • •Reported unstable cardiovascular disease, heart failure or symptomatic postural hypotension within 6 months before screening.
  • •Leg edema
  • •Inflammatory or progressive fibrotic disorder
  • •Renal insufficiency or failure
  • •History of infectious disorder.
  • •Chronic inflammatory disease
  • •History of stroke or myocardial infarction ( < 3 months).
  • •Bleeding or clotting disorder, use of oral anticoagulant therapy (heparin, warfarin).
  • •Lab values for
  • •Hemoglobin <10 g/dl.
  • •Platelet count <100,
  • •Prothrombin time/ partial thromboplastin time (PT/PTT)> 3 seconds.
  • •Alanine aminotrasferase (ALT) and aspartatet aminotrasferase (AST) > 1.5x of the normal lab value.
  • •Creatinine ≥ 1.4
  • •Poorly controlled diabetes (HbA1c ≥10)
  • •Bilirubin > 1.5x of the normal lab value.
  • •Systemic autoimmune disease.
  • •Receiving immunosuppressant medications.
  • •Uncontrolled hypertension or hypotension.
  • •Abdominal aortic aneurism > 5 cm.
  • •Active or untreated Tuberculosis.

研究组 & 干预措施

Platelet lysate injection

Experimental

Injection of platelet lysate intramuscularly in the gastrocnemius muscle

干预措施: Platelet lysate (Biological)

结局指标

主要结局

Assessment the safety of platelet lysate injection

时间窗: 6 months

Patients will be assessed for any relevant adverse event resulting from the platelet lysate injection

次要结局

  • Assessment the efficacy of platelet lysate injection(6 months)

研究者

申办方类型
Other
责任方
Principal Investigator
主要研究者

Moath AlSmady

Researcher

University of Jordan

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