Viewing Study NCT05965453



Ignite Creation Date: 2024-05-06 @ 7:19 PM
Last Modification Date: 2024-10-26 @ 3:04 PM
Study NCT ID: NCT05965453
Status: RECRUITING
Last Update Posted: 2023-07-28
First Post: 2023-06-27

Brief Title: Evaluation of the Castor Single Branch Stent Graft in Treatment of Acute Aortic Syndrome
Sponsor: First Affiliated Hospital Xian Jiaotong University
Organization: First Affiliated Hospital Xian Jiaotong University

Study Overview

Official Title: Real-world Experience With the Castor Single Branch Stent Graft in the Management of Acute Aortic Syndrome
Status: RECRUITING
Status Verified Date: 2023-06
Last Known Status: None
Delayed Posting: No
If Stopped, Why?: Not Stopped
Has Expanded Access: False
If Expanded Access, NCT#: N/A
Has Expanded Access, NCT# Status: N/A
Acronym: ECAAS
Brief Summary: The objective of this study to evaluate the safety and effectiveness of the Castor single branch stent graft for endovascular repair of acute aortic syndrome patients without an inadequate proximal landing zone 15mm
Detailed Description: The goal of this observational ambispective and multicenter cohort study is to evaluate efficacy and safety of the Castor single branch stent graft

205 patients who received thoracic endovascular aortic repair by meant of the Castor single branch stent graft from June 2018 to June 2022 were enrolled in our study All enrolled patients have an inadequate proximal landing zone 15mm and they underwent routine follow-up after thoracic endovascular aortic repair at 1-month 6-months and 1-year for the following but not limited to assessment physical examination laboratory test and the CT angiography

Meanwhile the enrolled patients will come for continuous follow-up at 2-years 3-years and annually to 10-years post-procedure

Study Oversight

Has Oversight DMC: None
Is a FDA Regulated Drug?: False
Is a FDA Regulated Device?: False
Is an Unapproved Device?: None
Is a PPSD?: None
Is a US Export?: None
Is an FDA AA801 Violation?: None