Viewing Study NCT04008550



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Last Modification Date: 2024-10-26 @ 1:13 PM
Study NCT ID: NCT04008550
Status: TERMINATED
Last Update Posted: 2020-08-05
First Post: 2019-06-26

Brief Title: Prognostic Impact of the Evolution of PAH 3 Months After TAVI HTP-TAVI
Sponsor: University Hospital Rouen
Organization: University Hospital Rouen

Study Overview

Official Title: Prognostic Impact of the Evolution of Pulmonary Arterial Hypertension 3 Months After Transcatheter Aortic Valve Implantation
Status: TERMINATED
Status Verified Date: 2020-08
Last Known Status: None
Delayed Posting: No
If Stopped, Why?: Delay in enrolment 24 at 1 year Lower than estimated prevalence of PAH 15 instead of 50 Refusal of patients with PAH to participate
Has Expanded Access: False
If Expanded Access, NCT#: N/A
Has Expanded Access, NCT# Status: N/A
Acronym: HTP-TAVI
Brief Summary: Aortic stenosis AS is the most frequent valvulopathy in Western countries The prevalence of AS is constantly increasing due to the aging of the population Several studies have shown that pulmonary arterial hypertension PAH was common in AS patients referred for TAVI and that it was an independent predictor of mortality after TAVI

Currently there is no data in the literature regarding the evolution and prognosis value of PAH measured using right heart catheterization reference method PAH could either regress after TAVI or continue to progress despite the treatment of valvulopathy resulting in a refractory right heart failure that can lead to death

The hypothesis of this study is that patients with PAH before TAVI procedure and at the 3-month follow-up visit PAH persistence have an increased risk of cardiovascular mortality compared to patients with no PAH at 3 months or having a significant reduction of their PAH PAH regression

The aim of the study is to evaluate the prognostic impact of the evolution of PAH after TAVI in 424 patients using right heart catheterization
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