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Clinical Trial Summary

To evaluate the efficacy and safety of peripheral shock catheter system in peripheral arterial angioplasty.This trial is a prospective, multicenter, open, randomized, parallel controlled and superior clinical trial. Select ≥3 hospitals with the qualification of national clinical trial institutions as clinical trial centers, and plan to enroll a total of 120 subjects. The ratio of subjects in the trial group and the control group is 1: 1 (60 in the trial group and 60 in the control group). This study mainly includes four stages: the screening (baseline) period (-14 ~0 days), the operation day (the day of treatment), the postoperative visit (0~7days ) and the 30-day follow-up (30 ±7days ).


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms


NCT number NCT05435716
Study type Interventional
Source Suzhou Zhonghui Medical Technology Co., Ltd.
Contact Sally Yan
Phone 18800263183
Email Sally.yan@hh-healthcare.com
Status Recruiting
Phase N/A
Start date August 5, 2021
Completion date September 8, 2023

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