Effects of Aortic Valve Replacement on Myocardial T1 Values in Severe Aortic Valve Stenosis

NCT ID: NCT05404100

Last Updated: 2023-11-18

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

RECRUITING

Total Enrollment

60 participants

Study Classification

OBSERVATIONAL

Study Start Date

2021-04-01

Study Completion Date

2024-04-01

Brief Summary

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Background: Severe aortic valve stenosis (AS) is the commonest valve disease. Aortic valve replacement (AVR) is primarily indicated when symptoms occur and/or when there is a drop in left ventricular ejection fraction. However, irreversible myocardial damage, such as replacement fibrosis, leads to increased morbidity and mortality despite treatment. Improved patient selection and timely treatment is thus warranted. T1 mapping, a non-invasive method to quantify myocardial fibrosis by cardiac magnetic resonance (CMR), could be a marker to guide treatment.

Aims: To investigate the change of myocardial fibrosis\* in AS patients following AVR and if these changes are associated with disease and/or procedural characteristics.

Methods: This is an observational clinical trial. Approximately 60 patients with severe AS planned to undergo AVR (either surgical or transcatheter) at Rigshospitalet, Denmark will be included. Participants will undergo CMR before surgery and at a 1-year follow-up. Other assessments include clinical evaluation and blood sampling. The primary end-point is change in T1 values after AVR.

Hypotheses and perspectives: The investigators hypothesize that (1) myocardial fibrosis\* will regress in patients undergoing AVR as a group, (2) the degree of myocardial fibrosis is positively correlated with the degree of symptoms, (3) the regression of myocardial fibrosis is greater in patients undergoing TAVR compared to SAVR, and (4) the regression of myocardial fibrosis is greater in patients with tricuspid aortic stenosis compared to bicuspid aortic stenosis. Ultimately, T1 mapping is a potential marker for improved patient selection for the timing of AVR.

\* Estimated by T1 mapping

Detailed Description

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Conditions

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Aortic Valve Stenosis Aortic Valve Replacement Myocardial Fibrosis Cardiac Magnetic Resonance T1 Mapping

Study Design

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Observational Model Type

CASE_ONLY

Study Time Perspective

PROSPECTIVE

Study Groups

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Severe aortic valve stenosis

Patients with severe AS planned to undergo AVR, either as surgical aortic valve replacement (SAVR) or transcatheter aortic valve replacement (TAVR).

Aortic valve replacement

Intervention Type PROCEDURE

SAVR or TAVR

Interventions

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Aortic valve replacement

SAVR or TAVR

Intervention Type PROCEDURE

Eligibility Criteria

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Inclusion Criteria

* Age ≥ 18 years
* Severe aortic valve stenosis (Vmax \> 4 m/s and/or mean gradient \>40 mmHg)

Exclusion Criteria

* Reduced left ventricular ejection fraction (\<50%)
* More than mild left-sided valvular insufficiency
* Previous or planned primary coronary intervention (PCI) or coronary artery by-pass grafting (CABG)
* Persistent atrial fibrillation
* Contraindications for CMR (pregnancy, severe claustrophobia, magnetic metallic implants)
* Pacemaker/ICD
Minimum Eligible Age

18 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

No

Sponsors

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Danish Cardiovascular Academy (DCA)

UNKNOWN

Sponsor Role collaborator

Eva og Henry Frænkels Mindefond

OTHER

Sponsor Role collaborator

Snedkermester Sophus Jacobsen and hustru Astrid Jacobsens Foundation

OTHER

Sponsor Role collaborator

Rigshospitalet, Denmark

OTHER

Sponsor Role lead

Responsible Party

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Katrine Aagaard Myhr

Principtal Investigator

Responsibility Role PRINCIPAL_INVESTIGATOR

Locations

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Rigshospitalet

Copenhagen O, , Denmark

Site Status RECRUITING

Countries

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Denmark

Central Contacts

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Katrine A Myhr, MD

Role: CONTACT

+4571120280

Redi Pecini, MD, PhD

Role: CONTACT

Facility Contacts

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Katrine A Myhr, MD

Role: primary

+4571120280

Other Identifiers

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H-20029458

Identifier Type: -

Identifier Source: org_study_id

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