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Evaluation of Mitral Valve Insufficiency Under General Anesthesia (MITIGATE)

A

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

Status

Enrolling

Conditions

Mitral Valve Disease
Mitral Valve Insufficiency
Mitral Regurgitation

Study type

Observational

Funder types

Other

Identifiers

NCT05736289
W22_423

Details and patient eligibility

About

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

Enrollment

50 estimated patients

Sex

All

Ages

18+ years old

Volunteers

No Healthy Volunteers

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

Trial design

50 participants in 2 patient groups

Percutaneous mitral valve repair
Description:
Patients undergoing percutaneous mitral valve repair under general anesthesia for mitral valve regurgitation.
Surgical mitral valve repair or replacement
Description:
Patients undergoing surgical mitral valve repair or replacement for mitral valve regurgitation.

Trial contacts and locations

1

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Central trial contact

Johan TM Tol, MD; Denise P Veelo, MD PhD

Data sourced from clinicaltrials.gov

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