Viewing Study NCT04861389



Ignite Creation Date: 2024-05-06 @ 4:05 PM
Last Modification Date: 2024-10-26 @ 2:03 PM
Study NCT ID: NCT04861389
Status: UNKNOWN
Last Update Posted: 2021-04-27
First Post: 2020-11-29

Brief Title: Distal Transradial Access for Primary Percutaneous Coronary Intervention in STEMI Patients
Sponsor: Shenzhen Peoples Hospital
Organization: Shenzhen Peoples Hospital

Study Overview

Official Title: The Comparison of Distal Transradial Access and Transradial Access for Primary Percutaneous Coronary Intervention in STEMI PatientsRESERVE Trial A Single-center Open Prospective Randomized Controlled Trial
Status: UNKNOWN
Status Verified Date: 2021-04
Last Known Status: 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: RESERVE
Brief Summary: The transradial access TRA is currently the preferred approach for percutaneous coronary intervention PCI However in patients with ACUTE ST-segment elevation myocardial infarction STEMI after emergency PCI the high incidence of THE radial artery RAO limits the future choice of the radial artery for percutaneous intervention The literature reported that distal transradial access dTRA significantly reduced RAO after elective PCI but the application of dTRA in emergency PCI in STEMI has not been reported We have completed 126 cases of dTRA undergoing emergency PCI after STEMI which has been preliminarily confirmed to be safe and effective A single-center open prospective randomized controlled study is planned to compare the use of dTRA and TRA in emergency PCI in STEMI patients The primary endpoint was the INCIDENCE of RAO within 24 hours after surgery This clinical study verified that dTRA compared with TRA could reduce the RAO incidence of STEMI patients after emergency PCI The project will explore a new artery approach to reduce RAO and provide a basis for the selection of artery approach in STEMI emergency PCI patients
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