Evaluation of Mitral Valve Insufficiency Under General Anesthesia

Academisch Medisch Centrum - Universiteit van Amsterdam (AMC-UvA)50 enrolled

Overview

Observational study in adult humans undergoing surgical or cardiological intervention for mitral valve insufficiency. Investigators aim to evaluate hemodynamic changes on an arterial pressure waveform level in patients before and after mitral valve intervention using Nexfin (BMEYE, Amsterdam, the Netherlands) continuous non-invasive hemodynamic monitoring, using finger cuff based technology to register beat-to-beat data

Study Type

OBSERVATIONAL

Enrollment

Conditions

Mitral Regurgitation Mitral Valve Disease Mitral Valve Insufficiency

Eligibility

Sex: ALLMin age: 18 Years

Medical Language ↔ Plain English

Inclusion Criteria: * All patients with moderate or severe mitral valve insufficiency undergoing cardiothoracic surgery or percutaneous treatment for this condition * Adult patients (\>18 years) Exclusion Criteria: * No informed consent

Locations (1)

Amsterdam University Medical Center

Amsterdam, Netherlands

RECRUITING

Outcomes

Primary Outcomes

Arterial pressure waveform changes

Arterial pressure waveform as recorded by a continuous non invasive hemodynamic monitoring system.

Time frame: Before and during general anesthesia for mitral valve repair or replacement, ranging from 1 to 5 hours.

Central Contacts

Johan TM Tol, MD

CONTACT

020 566 6478 j.tol2@amsterdamumc.nl

Denise P Veelo, MD PhD

CONTACT

020 566 6478 d.p.veelo@amsterdamumc.nl

Data from ClinicalTrials.gov

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