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临床试验/CTRI/2009/091/000590
CTRI/2009/091/000590招募中1 期

Stem cell therapy- Cellular Cardio myoplasty for patients with severe ventricular dysfunction

Frontier Lifeline PvtLtd0 个研究点目标入组 90 人开始时间: 待定最近更新:

试验速览

阶段
1 期
状态
招募中
发起方
入组人数
90

研究概览

简要总结

暂无简介。

研究设计

研究类型
Interventional

入排标准

入选标准

  • Patients aged between 0 to 60 years presenting with Dilated Cardiomyopathy or coronary artery disease (CAD) are enrolled. Patients with ventricular ejection fraction (LVEF) less than 35% are eligible for enrollement.

排除标准

  • 1. Sustained ventricular tachycardia in a 24 hour ECG.
  • 2. Chronic atrial fibrillation.
  • 3. Less than 6 months since last episode of cerebral
  • infarction.
  • 4. Less than 6 months since last coronary angioplasty or
  • less than 3 months since last bypass surgery.
  • 5. Patients with unstable angina, with a treatment rating
  • of 3 in the Braunwald system, but a severity of III and a
  • clinical rating of B or C.
  • 6. Presence of left ventricular thrombus by
  • echocardiography.
  • 7. Patient with a malignant tumour.
  • 8. Patient with diabetic proliferating retinopathy** (new
  • Fukuda classification BI to BV).
  • 9. Patients with chronic rheumatoid arthritis.
  • 10. Patient with haematological disease (leukaemia,
  • myeloproliferative disease or myelodysplastic
  • 11. Patients for whom cranial MRA reveals cerebral
  • 12. Patients for whom abdominal CT or ultrasonography
  • reveals splenomegaly.
  • 13 Patients with cirrhosis of the liver.
  • 14. Patients who cannot discontinue warfarin.
  • 15. AST (GOT) exceeding 100 IU/L or ALT (GPT)
  • exceeding 100 IU/L.
  • 16. Patients for whom it is impossible to perform both
  • cardiac MRI and left ventriculography (LVG).
  • 17. Any other reason that the Clinical supervisors or
  • clinical Researchers may have for considering a case
  • unsuitable for the study.

研究者

发起方
Frontier Lifeline PvtLtd

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