Viewing Study NCT06446102



Ignite Creation Date: 2024-06-16 @ 11:50 AM
Last Modification Date: 2024-10-26 @ 3:31 PM
Study NCT ID: NCT06446102
Status: COMPLETED
Last Update Posted: 2024-06-10
First Post: 2024-05-17

Brief Title: Bifurcation Coronary Lesion 0-0-1
Sponsor: RCFICPS
Organization: RCFICPS

Study Overview

Official Title: Bifurcation Coronary Lesion 0-0-1
Status: COMPLETED
Status Verified Date: 2024-06
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: Research Involving Human Persons RIHP 3 focusing on the treatment of type 0-0-1 bifurcation lesions in routine practice Multicenter Study

To retrieve and analyze the details of different angioplasty techniques used in this type of bifurcation lesion Medina 0-0-1 in order to describe current practice and search for predictors of clinical events
Detailed Description: The primary objective of the trial is to estimate the frequency of Major Adverse Cardiac Events MACE including cardiac death myocardial infarction within the territory of the treated lesion and revascularization of the target lesion in a representative population of patients treated by coronary angioplasty of type 0-0-1 bifurcation lesions

The sample size will be determined by the number of angioplasties of type 0-0-1 bifurcation lesions performed at each center between 2016 and 2022

Since the trial is observational in nature and there are no previously published studies the sample size cannot be calculated based on the desired precision of the estimation

Furthermore the purpose of the study is also to assess the techniques used to treat this type of coronary bifurcation and to highlight any differences between different centers and with other types of coronary bifurcation lesions described in the literature

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