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Clinical Trial Summary

The purpose of this study is to evaluate the efficacy and safety of IBD stent of Shenzhen Xianjian Company and IBE stent of American Gore company in the treatment of abdominal aortic aneurysm/iliac aneurysm reconstruction of internal iliac artery


Clinical Trial Description

This study is a prospective observational exploratory cohort study without a control group. As a single-group target value validation study, the main evaluation indicator is the primary patency rate one year after surgery. As an exploratory study, considering the enrollment ability to facilitate data analysis, 40 subjects are enrolled in the final study, and 20 are expected to be included in each study. All enrolled patients will be followed for 12 months for CTA to assess primary patency. Telephone follow-up was conducted at 1, 3, 6, and 12 months for adverse events. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT06162273
Study type Observational
Source RenJi Hospital
Contact Guanhua Xue, M.D.
Phone 13585785270
Email guanhuaxue@yeah.net
Status Not yet recruiting
Phase
Start date December 1, 2023
Completion date December 1, 2026

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