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The Role of PESP-PG in the Evaluation of the Severity of Low-Gradient Aortic Valve Stenosis in Patients with Atrial Fibrillation

The Role of PESP-PG in the Evaluation of the Severity of Low-Gradient Aortic Valve Stenosis in Patients with Atrial Fibrillation

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
DRKS
Registry ID
DRKS00034957
Enrollment
50
Registered
2024-09-20
Start date
2024-11-15
Completion date
Unknown
Last updated
2026-06-01

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

I35.0 I48.2

Interventions

Group 1: Patients with LG-AKS (KÖF = 1 cm² / MPG < 40 mmHg) and VHF are undergo invasive diagnostics via right/left heart catheterization. This involves simultaneous LV/Ao pressure measurement using t

Sponsors

Klinikum Byreuth
Lead Sponsor

Eligibility

Sex/Gender
All
Age
19 Years to No maximum

Inclusion criteria

Inclusion criteria: - Patients with echocardiographically proven LG-AKS (AVA = 1qcm (valve orifice area), MPG 50% or LVEF < 50%). - Atrial fibrillation. - Patients in whom a cardiac-CT is indicated to measure the Agatston score.

Exclusion criteria

Exclusion criteria: - AVA > 1 qcm, MPG = 40mmHg. - Patients in whom simultaneous LV-Ao pressure measurement is not possible due to access problems. - Inadequate analysis of pressure curves. - LVOT obstruction. - Unstable patients (tachycardia, hypotension, angina...). - Mechanical aortic valve replacement. - Untreated relevant coronary heart disease (e.g. severe coronary three-vessel disease, significant left main stenosis, proximal LAD stenosis, high-grade ostial stenosis, ...). - Detection of thrombi in the left ventricle or in the left atrium/-atrial appendage. - Patients in whom a cardiac-CT is not indicated to measure the Agatston score.

Design outcomes

Primary

MeasureTime frame
The primary endpoint is a PESP-PG = 40mmHg, which is measured invasively as follows: A VES is induced using a pigtail catheter (in the LV). The measurement is performed via simultaneous LV/Ao pressure registration and is analyzed using hemodynamic software (Siemens).

Secondary

MeasureTime frame
no secondary endpoints

Countries

Germany

Contacts

Public ContactTaki Eddine Sid

Klinikum Bayreuth

TakiEddine.Sid@klinikum-bayreuth.de+49921 400-6502

Outcome results

None listed

Source: DRKS (via WHO ICTRP) · Data processed: Jun 11, 2026