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Clinical Trial Summary

to detect the efficiency and safety of intravenous rtPA combined with RIPC in acute ischemic stroke patients


Clinical Trial Description

Remote ischemic post-conditioning, which consists of several brief cycles of intermittent ischemia-reperfusion of the arm or leg, may potentially confer a powerful systemic protection against prolonged ischemia in a distant organ. Numerous reports have confirmed it strongest endogenous neuroprotection against brain injury after stroke. Ren et al demonstrated that remote ischemic post-conditioning (RIPC) performed in the hind limbs can not only significantly reduce the stroke volume within 3 hours in rat model, but also ameliorate the outcome of the behavioral test. A long-term repeated RIPC therapy can also help improving neurological functions. A combination of RIPC and tPA can help with neuroprotection which improves the neurological functions. Thus, it is meaningful to transform these basic experimental results to the clinical treatment. In the RECAST-1 trial, RIC has shown it safety and efficiency in AIS patients without tPA. However, there is no further explanation for the patients with IVT. Thus, in this study, we aim to demonstrate the efficiency and safety of RIPC in AIS patients performed rt-PA within 4.5 hours. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT02886390
Study type Interventional
Source Capital Medical University
Contact Xunming Ji, MD. PhD
Phone +86-10-83198952
Email jixm@ccmu.edu.cn
Status Recruiting
Phase N/A
Start date June 16, 2018
Completion date May 2019

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