Time reduction by single catheter PCI method for patients with acute myocardial infarctio

Phase 4

Recruiting

• Conditions: ST elevation myocardial infarction

• Registration Number: JPRN-UMIN000049578
• Lead Sponsor: Tokai University

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Results First Posted: 1900-01-01
• Study Start: 2022-12-01
• Last Update Posted: 17 October 2023
• Study Completion: 2024-12-20

Recruitment & Eligibility

• Status: Recruiting
• Sex: All
• Target Recruitment: 400

Inclusion Criteria

Not provided

Exclusion Criteria

Patients with shock requiring insertion of Impella, ECMO or IABP before PCI Patients requiring cardiopulmonary resuscitation due to cardiac arrest Patients requiring temporary pacemaker due to bradycardia Patients undergoing dialysis Patients judged by the attending physician to be inappropriate for registration

Study & Design

• Study Type: Interventional
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
Sheath-to-first device activation time Time from insertion of sheath to reperfusion treatment apparatus (First device activation)

Secondary Outcome Measures

Name	Time	Method
*Door-to-balloon time *Total ischemia time * Fluoroscopy time and fluoroscopy dose * Amount of contrast medium * Number of catheters used * Hospital expense * All-cause mortality and cardiovascular mortality at 30 days * Hemorrhagic complication rate at 30 days * All-cause mortality and cardiovascular mortality at 1 year * Success rate of SC-PCI method