Viewing Study NCT05903560



Ignite Creation Date: 2024-05-06 @ 7:07 PM
Last Modification Date: 2024-10-26 @ 3:01 PM
Study NCT ID: NCT05903560
Status: RECRUITING
Last Update Posted: 2023-08-01
First Post: 2023-06-06

Brief Title: Radial Versus Femoral Access For Thrombectomy in Patients With Acute Basilar Artery Occlusion
Sponsor: Jinling Hospital China
Organization: Jinling Hospital China

Study Overview

Official Title: Radial Versus Femoral Access For Thrombectomy in Patients With Acute Basilar Artery Occlusion
Status: RECRUITING
Status Verified Date: 2023-07
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: None
Brief Summary: Stroke is one of the most important diseases endangering the health and quality of life of Chinese people Acute ischemic stroke AIS is commonly caused by cerebrovascular stenosis or occlusion The most effective treatment for AIS is timely and successful angiographic reperfusion

Due to the large diameter and obvious positioning of bilateral femoral arteries the transfemoral artery TFA using Seldingers technique has been the most commonly used approach for endovascular treatment However recent studies have suggested that the radial artery is an ideal puncture site for cerebrovascular intervention Small sample studies have confirmed that endovascular recanalization for acute anterior circulation large vessel occlusion via TRA has been safe and effective Still there are some complex approaches needed to be converted to TFA There has been no difference in total operation duration and fluoroscopy time between TRA and TFA but the TRA group had higher radiation dose and shorter hospital stays than the TFA group In addition TRA tends to be more convenient than TFA especially for posterior circulation lesions

However the current studies are based on a single center with a small sample size and there has been still a lack of large-sample randomized controlled experiments to verify the safety and effectiveness of posterior endovascular recanalization via TRA
Detailed Description: None

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