Trial Number

965-19

Age range

18 Years to 90 Years

Gender

Male or Female

Enrolling Patients

Yes

A prospective, single-arm, non-blinded study, intending to collect and evaluate data in up to forty (40) human subjects with acute thrombosis, treated with the CAPERE™ Thrombectomy System. The CAPERE™ Thrombectomy System is designed to achieve clot retrieval with one (1) treatment session. The CAPERE™ system is cleared for market in the United States and this study is intended to capture real-world clinical data as part of CAPERE™ post-market clinical follow up.

Principal Investigator

MemorialCare Research Center Contact Form

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