Central Blood Pressure Evaluation In Interventional Valve Reconstructio

Recruiting

• Conditions: I35; I34; Nonrheumatic aortic valve disorders; Nonrheumatic mitral valve disorders

• Registration Number: DRKS00011289
• Lead Sponsor: Medizinische Klinik III, Herzzentrum des Universitätsklinikums Köln, Hypertoniezentrum

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Study Start: 2017-01-19
• Last Update Posted: 19 August 2024

Recruitment & Eligibility

• Status: Recruiting
• Sex: All
• Target Recruitment: 450

Inclusion Criteria

given informed consent
-recieving TAVI, MitraClip or left heart catheterization in clinical routine

Exclusion Criteria

contraindications against simultanous blood pressure measurements on both arms (dialysis shunt, mamma-CA and others)

systolic blood pressure difference >15 mmHg of both arms

Study & Design

• Study Type: observational
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
This study aims at improving the understanding in short to midterm changes in hemodynamics in patients undergoing interventional valve reconstruction and replacement. These data compared to baseline parameters and clinical evaluation may lead to a better risk stratificiation regarding preiprocedural complications and outcomes.