Ignite Creation Date:
2024-05-06 @ 6:00 PM
Last Modification Date:
2024-10-26 @ 2:40 PM
Study NCT ID:
NCT05514210
Status:
NOT_YET_RECRUITING
Last Update Posted:
2023-06-07
First Post:
2022-08-22
Brief Title:
Feasibility and Effectiveness of a Real-time Heart Team Approach in Complex CAD
Sponsor:
China National Center for Cardiovascular Diseases
Organization:
China National Center for Cardiovascular Diseases
Study Overview
Official Title:
Feasibility and Effectiveness of a Real-time Heart Team Approach in Complex Coronary Artery Disease
Status:
NOT_YET_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:
None
Brief Summary:
This study is aimed to evaluate the clinical outcomes efficiency and feasibility of the real-time heart team approach and the conventional heart team approach
Detailed Description:
This study is a multicenter randomized controlled trial According to the inclusion and exclusion criteria patients with complex coronary artery disease undergoing elective coronary angiography will be prospectively enrolled in the study Patients will be randomly assigned to the real-time heart team group and the conventional heart team group by block randomization The real-time heart team group needs to conduct multidisciplinary heart team discussion during the coronary angiography process while the traditional heart team group needs to conduct multidisciplinary heart team discussion offline and face-to-face after the coronary angiography process Patients who are not randomized will be registered This study will prospectively collect the patient information heart team meeting process clinical treatment and clinical outcomes to evaluate the efficiency and feasibility and differences in clinical outcomes of patients under different heart team approaches
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