Viewing Study NCT06341166



Ignite Creation Date: 2024-05-06 @ 8:20 PM
Last Modification Date: 2024-10-26 @ 3:25 PM
Study NCT ID: NCT06341166
Status: RECRUITING
Last Update Posted: 2024-04-02
First Post: 2024-03-14

Brief Title: Multiparametric SCores for Prediction of Myocardial fIbrosis in Patients With MITral vAlve pRolapse
Sponsor: Centro Cardiologico Monzino
Organization: Centro Cardiologico Monzino

Study Overview

Official Title: Multiparametric SCores for Prediction of Myocardial fIbrosis in Patients With MITral vAlve pRolapse the SCIMITAR Trial
Status: RECRUITING
Status Verified Date: 2024-03
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: SCIMITAR
Brief Summary: This is a multicenter observational prospective and retrospective study which aims are 1 to compute a scoring model potentially predictive for the diagnosis of fibrosis by CMR in patients with MVP 2 to identify specific features that may predispose to mild VAs or SCD in patients with MVP
Detailed Description: Patients with mitral valve prolapse and non-significant mitral regurgitation generally have a good prognosis A minority of patients with MVP suffers from ventricular arrhythmias Different demographic clinical and electrocardiographic characteristics as well as morphological and structural features of the MV were described as potential risk factors for ventricular arrhythmias among which fibrosis of the left ventricular inferolateral wall and posterior papillary muscle as detected by cardiac magnetic resonance

As cardiac magnetic resonance has some limitations it is unknown if and which patients with mitral valve prolapse should undergo cardiac magnetic resonance in routine clinical practice to search for late gadolinium enhancement as a surrogate for myocardial fibrosis

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