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临床试验/NCT01271309
NCT01271309已完成不适用

Migratory and Angiogenic Dysfunction of Circulating CD133 Stem Cells: a New Prognostic Marker in Myocardial Ischemia.

IRCCS Multimedica2 个研究点 分布在 1 个国家目标入组 170 人开始时间: 2007年7月最近更新:
适应症

试验速览

阶段
不适用
状态
已完成
发起方
入组人数
170
试验地点
2
主要终点
Prognostic value of CD133+ stem cells in MI

研究概览

简要总结

The present project aims to determine whether a deficit in migration of stem cells could be implicated in the failure to mount an adequate collateralization after Myocardial Infarction (MI) and thereby facilitate the development of post-ischemic heart failure (HF) and to dissect underlying molecular mechanisms. Furthermore, the investigators wish to determine the predictive value of stem cell migration assay in patients with MI.

详细描述

MAIN OBJECTIVES OF THE STUDY:

Characterization of circulating CD133+ stem cells in a group of 170 patients with MI (mean post-MI follow up, 6 months):

  • Counting total mononuclear cells and FACS analysis of CD133 stem cells.
  • Characterization of CD133+ stem cell biology: Migratory assay, imaging of cytoskeleton, angiogenesis tests in vitro.
  • Evaluation of migratory signalling, with specific focus on the PI3K/Akt/eNOS system.

Assessment of the prognostic value of the stem cell migration assay.

  • Relationship between cell biology tests on CD133+ cells and changes in circulating cytokines and pro-angiogenic factors after MI.
  • Assessment of area at risk by ECG-synchronized Single Photon Emission Computed Tomography (gated-SPECT) in subgroups with different patterns of stem cell migratory tests.
  • Assessment of ventricular remodelling (echocardiography, NMR) in relation with patterns of stem cell migratory test.

研究设计

研究类型
Observational
观察模型
Cohort
时间视角
Prospective

入排标准

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

入选标准

  • Age >= 18 years
  • Thoracic pain lasting at least 20 min and ST changes or left B block, not present in previous ECG.
  • MI confirmed by elevation of troponin I and CK-MB.
  • Patients with Killip II e III LV dysfunction will be included.

排除标准

  • Patients reporting thoracic pain 24 hours prior to hospitalization
  • HF symptoms resistant to therapy
  • Haemoglobin< 10 gr/dl
  • Haemodynamic instability (systolic pressure <90 mmHg after treatment)
  • Alterations in haematopoiesys
  • Concurrent neoplastic disease
  • No written informed consent or other conditions that affect patient's compliance to protocol.

结局指标

主要结局

Prognostic value of CD133+ stem cells in MI

时间窗: 12 months

Correlation of clinical parameters of disease evolution and biological features

次要结局

  • Correlation of disease evolution and other biomarkers(12 months)

研究者

发起方
IRCCS Multimedica
申办方类型
Other
责任方
Sponsor

研究点 (2)

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