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Clinical Trial Summary

To evaluate the safety and efficacy of R.A.V.I.(radial access for abdominopelvic vascular intervention), and evaluate the feasibility and safety of repeated radial artery intervention


Clinical Trial Description

This is a prospective, multicenter clinical study with 1143 patients scheduled to enroll based on data from 10 hospitals for any abdominopelvic vascular intervention that can be performed via a radial approach。 The investigators conducted abdominopelvic vascular interventional therapy via radial artery approach according to the lesions and conditions of the subjects. All subjects underwent Barbeau tests before surgery to examine the flow traffic of the radial and ulnar arteries, and to measure the diameter of the radial artery (inner diameter) by Doppler ultrasound to evaluate its compatibility with the outer diameter of the vascular sheath. All enrolled subjects were followed up within 24 hours and 1 month after unsheathing to observe the clinical outcome of patients. ;


Study Design


Related Conditions & MeSH terms

  • Vascular Access Device Complications

NCT number NCT05956860
Study type Observational
Source Zhongda Hospital
Contact Hai-Dong Zhu, MD
Phone +862583262224
Email zhuhaidong9509@163.com
Status Recruiting
Phase
Start date August 7, 2023
Completion date December 30, 2025

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