Viewing Study NCT05255939



Ignite Creation Date: 2024-05-06 @ 5:17 PM
Last Modification Date: 2024-10-26 @ 2:25 PM
Study NCT ID: NCT05255939
Status: UNKNOWN
Last Update Posted: 2022-02-25
First Post: 2022-01-17

Brief Title: Decrease Artery Occlusion by Distal Radial Arterial Cannulation in ACS Patients
Sponsor: Shenzhen Peoples Hospital
Organization: Shenzhen Peoples Hospital

Study Overview

Official Title: Decrease Artery Occlusion by Distal Radial Arterial Cannulation in ACS Patients
Status: UNKNOWN
Status Verified Date: 2022-02
Last Known Status: NOT_YET_RECRUITING
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: DONATION
Brief Summary: The site of arterial access for coronary angiography and intervention has been the focus of research for decades as it is the source of major complications Transradial access TRA reduces complications among patients undergoing percutaneous coronary procedures but is reported with the complication of radial artery occlusion RAO that limits the radial artery for future needs

Distal radial access dTRA has recently gained global popularity as an alternative access route for vascular procedures Among the benefits of dTRA are the low risk of entry site bleeding complications the low rate of radial artery occlusion and improved patient and operator comfort

This study aims to reveal the feasibility and safety of dTRA and routine TRA procedures in acute coronary syndrome patients The primary endpoints are forearm radical occlusion rate and major adverse cardiovascular events MACEs in the two groups respectively Investigators will also focus on puncture success in diagnostic and interventional cases rate of One attempt success access time procedure time crossover rate contrast dose of patients fluoroscopy time and dose and healthcare cost of each group
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