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Early Versus Deferred Aortic Valve Replacement in Patients With Moderate Aortic Stenosis and Mitral Regurgitation (TIAMAR)

Primary Purpose

Aortic Valve Replacement in Patients With Moderate Aortic Stenosis Combined With Mitral Regurgitation

Status
Recruiting
Phase
Not Applicable
Locations
Switzerland
Study Type
Interventional
Intervention
Transcatheter or surgical aortic valve replacement with or without transcatheter or surgical mitral valve repair/replacement
Deferred treatment, with intervention once AVA is ≤1.0 cm2 or if concomitant mitral regurgitation meets an indication for intervention
Sponsored by
Insel Gruppe AG, University Hospital Bern
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Aortic Valve Replacement in Patients With Moderate Aortic Stenosis Combined With Mitral Regurgitation

Eligibility Criteria

18 Years - undefined (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • Age ≥18 years
  • Moderate native aortic stenosis defined by an aortic valve area (AVA) ≤1.5 cm2 and >1.0 cm2 and transvalvular mean gradient ≥20 mmHg and <40 mmHg.
  • Primary or secondary mitral regurgitation (at least moderate) defined by effective regurgitant orifice area (EROA) ≥20 mm2 or regurgitant volume ≥30 ml
  • New York Heart Association (NYHA) functional class ≥2

Exclusion Criteria:

  • Life expectancy <1 year irrespective of valvular heart disease
  • Left ventricular ejection fraction <30% or LVESD >70mm
  • Echocardiographic evidence of severe right ventricular dysfunction
  • Untreated clinically significant CAD requiring revascularisation
  • Moderate or severe aortic regurgitation
  • Severe tricuspid valve disease requiring intervention
  • Symptomatic patients with severe primary MR who are operable and not high risk
  • Patients with severe secondary MR who remain symptomatic despite optimal medical therapy and who are judged appropriate for transcatheter edge-to-edge repair or surgery by the Heart Team
  • Transcatheter or surgical treatment of valvular and/or coronary artery disease within 90 days prior to randomization
  • COPD with home oxygen therapy
  • Estimated or measured systolic PAP >70 mmHg
  • Stroke within 30 days prior to the randomization
  • Inability to provide written informed consent
  • Participation in another cardiovascular trial before reaching the primary endpoint.

Sites / Locations

  • Insel Gruppe AG, Inselspital BernRecruiting
  • University Hospital Geneva (HUG)Recruiting

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

Other

Arm Label

Early transcatheter or surgical aortic valve replacement

Control Intervention

Arm Description

Early transcatheter or surgical aortic valve replacement with or without transcatheter or surgical mitral valve repair/replacement.

Deferred treatment, with intervention once AVA is ≤1.0 cm2 or if concomitant mitral regurgitation meets an indication for intervention.

Outcomes

Primary Outcome Measures

The primary outcome will be a composite of all-cause death, stroke, and unplanned hospitalization for heart failure related to valvular heart disease at 2 years.

Secondary Outcome Measures

All-cause death
Number of all-cause death within study participation
Cardiovascular death
Number of patients with Cardiovascular death within study participation
Neurologic events
Number of patients with stroke, symptomatic hypoxic-ischaemic injury, TIA and evaluation
Hospitalization for heart failure
Number of patients who need hospitalization for heart failure within study participation and evaluation
New-onset atrial fibrillation
Number of patients with new-onset atrial fibrillation within study participation and evaluation
Implantation of a permanent pacemaker
Number of patients with atrioventricular conductance disturbance requiring the implantation of a permanent pacemaker
Aortic or mitral valve re-intervention
Number of patients with Aortic or mitral valve re-intervention within study participation and evaluation
NYHA functional class
Measurement of NYHA functional class within study participation
Days alive out of hospital (DAOH)
Calculation of days alive out of hospital (DAOH) within study participation
The evaluation Health-related quality of life assessment by means of the KCCQ 12 questionnaire
Record the health-related quality of life assessment by means of the KCCQ 12 questionnaire within study participation

Full Information

First Posted
March 25, 2022
Last Updated
February 8, 2023
Sponsor
Insel Gruppe AG, University Hospital Bern
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1. Study Identification

Unique Protocol Identification Number
NCT05310461
Brief Title
Early Versus Deferred Aortic Valve Replacement in Patients With Moderate Aortic Stenosis and Mitral Regurgitation
Acronym
TIAMAR
Official Title
Early Versus Deferred Aortic Valve Replacement in Patients With Moderate Aortic Stenosis Combined With Mitral Regurgitation: a Randomized Clinical Trial
Study Type
Interventional

2. Study Status

Record Verification Date
February 2023
Overall Recruitment Status
Recruiting
Study Start Date
August 17, 2022 (Actual)
Primary Completion Date
July 1, 2024 (Anticipated)
Study Completion Date
January 1, 2030 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Insel Gruppe AG, University Hospital Bern

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
No

5. Study Description

Brief Summary
The aim of the present study is to investigate safety and efficacy of early versus deferred aortic valve replacement in patients with moderate aortic stenosis combined with moderate mitral regurgitation.
Detailed Description
In more than one-half of all patients with valvular heart disease, more than a single valve is involved. Valvular aortic stenosis coexists with significant mitral valve disease in up to one-third of patients undergoing aortic valve replacement (AVR). Guidelines for the management of valvular heart disease provide recommendations for isolated valvular lesions; data to guide timing of intervention in patients with multivalvular disease is however scarce. Currently, patients with moderate aortic stenosis (AS) in combination with mitral regurgitation have an indication for aortic valve replacement (AVR) only if the concomitant mitral regurgitation meets an indication for surgery. However, the hemodynamic stress of combined valvular lesions is greater than its individual components, and patients may benefit from early intervention. Furthermore, the presence of multivalvular heart disease complicates the assessment of individual valvular lesions. In patients with combined AS and mitral regurgitation (MR), increased left ventricular pressure exacerbates the mitral regurgitant volume. Conversely, decreased forward flow across the aortic valve underestimates the severity of aortic stenosis when assessed by a pressure gradient. Standard cut-off values inadequately reflect the hemodynamic stress in concomitant aortic and mitral valve disease, and recommendations for the timing of valvular replacement fail to account for the complex interplay of multiple valvular lesions. Timing of intervention in patients with combined AS and MR is therefore challenging and evidence on the optimal timing of intervention is scarce. Thus, the objective of the present study is to investigate safety and efficacy of early versus deferred aortic valve replacement in patients with moderate aortic stenosis combined with at least moderate mitral regurgitation. Patients with combined aortic stenosis and mitral regurgitation will be screened for eligibility. If eligible and informed consent is provided, patients will be randomly allocated in a 1:1 ratio to early (within 3 months) or deferred aortic valve replacement (with or without mitral valve intervention).

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Aortic Valve Replacement in Patients With Moderate Aortic Stenosis Combined With Mitral Regurgitation

7. Study Design

Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
None (Open Label)
Allocation
Randomized
Enrollment
80 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
Early transcatheter or surgical aortic valve replacement
Arm Type
Experimental
Arm Description
Early transcatheter or surgical aortic valve replacement with or without transcatheter or surgical mitral valve repair/replacement.
Arm Title
Control Intervention
Arm Type
Other
Arm Description
Deferred treatment, with intervention once AVA is ≤1.0 cm2 or if concomitant mitral regurgitation meets an indication for intervention.
Intervention Type
Procedure
Intervention Name(s)
Transcatheter or surgical aortic valve replacement with or without transcatheter or surgical mitral valve repair/replacement
Intervention Description
Early transcatheter or surgical aortic valve replacement with or without transcatheter or surgical mitral valve repair/replacement.
Intervention Type
Procedure
Intervention Name(s)
Deferred treatment, with intervention once AVA is ≤1.0 cm2 or if concomitant mitral regurgitation meets an indication for intervention
Intervention Description
Deferred transcatheter or surgical aortic valve replacement with or without transcatheter or surgical mitral valve repair/replacement.
Primary Outcome Measure Information:
Title
The primary outcome will be a composite of all-cause death, stroke, and unplanned hospitalization for heart failure related to valvular heart disease at 2 years.
Time Frame
2 years
Secondary Outcome Measure Information:
Title
All-cause death
Description
Number of all-cause death within study participation
Time Frame
5 years
Title
Cardiovascular death
Description
Number of patients with Cardiovascular death within study participation
Time Frame
5 years
Title
Neurologic events
Description
Number of patients with stroke, symptomatic hypoxic-ischaemic injury, TIA and evaluation
Time Frame
5 years
Title
Hospitalization for heart failure
Description
Number of patients who need hospitalization for heart failure within study participation and evaluation
Time Frame
5 years
Title
New-onset atrial fibrillation
Description
Number of patients with new-onset atrial fibrillation within study participation and evaluation
Time Frame
5 years
Title
Implantation of a permanent pacemaker
Description
Number of patients with atrioventricular conductance disturbance requiring the implantation of a permanent pacemaker
Time Frame
5 years
Title
Aortic or mitral valve re-intervention
Description
Number of patients with Aortic or mitral valve re-intervention within study participation and evaluation
Time Frame
5 years
Title
NYHA functional class
Description
Measurement of NYHA functional class within study participation
Time Frame
5 years
Title
Days alive out of hospital (DAOH)
Description
Calculation of days alive out of hospital (DAOH) within study participation
Time Frame
5 years
Title
The evaluation Health-related quality of life assessment by means of the KCCQ 12 questionnaire
Description
Record the health-related quality of life assessment by means of the KCCQ 12 questionnaire within study participation
Time Frame
5 years
Other Pre-specified Outcome Measures:
Title
Major vascular complications (VARC-3)
Description
Number of patients with major vascular complications within the study population and evaluation
Time Frame
5 years
Title
Cardiac structural complications (major, minor) (VARC-3)
Description
Number of patients with cardiac structural complications within the study population and evaluation
Time Frame
5 years
Title
Cerebrovascular events (disabling and non-disabling stroke, and TIA) (VARC-3)
Description
Number of patients with Cerebrovascular events (disabling and non-disabling stroke, and TIA) (VARC-3) within the study population and evaluation
Time Frame
5 years
Title
Myocardial infarction
Description
Number of patients with Myocardial infarction within the study population and evaluation
Time Frame
5 years
Title
Acute kidney injury (VARC-3)
Description
Number of patients with acute kidney injury (VARC-3) within the study population and evaluation
Time Frame
5 years
Title
Access-related non-vascular major complications (VARC-3)
Description
Number of patients with access-related non-vascular major complications (VARC-3) within the study population and evaluation
Time Frame
5 years
Title
Bleeding type 3-5 (VARC-3)
Description
Record all bleeding type 3-5 (VARC-3) within the study population
Time Frame
5 years
Title
Prosthetic valve endocarditis
Description
Number of patients Prosthetic valve endocarditis within the study population
Time Frame
5 years
Title
Prosthetic valve thrombosis
Description
Number of patients prosthetic valve thrombosis within the study population
Time Frame
5 years
Title
Valve-related dysfunction requiring reintervention
Description
Number of patients valve-related dysfunction requiring reintervention within the study population
Time Frame
5 years

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Age ≥18 years Moderate native aortic stenosis defined by an aortic valve area (AVA) ≤1.5 cm2 and >1.0 cm2 and transvalvular mean gradient ≥20 mmHg and <40 mmHg. Primary or secondary mitral regurgitation (at least moderate) defined by effective regurgitant orifice area (EROA) ≥20 mm2 or regurgitant volume ≥30 ml New York Heart Association (NYHA) functional class ≥2 Exclusion Criteria: Life expectancy <1 year irrespective of valvular heart disease Left ventricular ejection fraction <30% or LVESD >70mm Echocardiographic evidence of severe right ventricular dysfunction Untreated clinically significant CAD requiring revascularisation Moderate or severe aortic regurgitation Severe tricuspid valve disease requiring intervention Symptomatic patients with severe primary MR who are operable and not high risk Patients with severe secondary MR who remain symptomatic despite optimal medical therapy and who are judged appropriate for transcatheter edge-to-edge repair or surgery by the Heart Team Transcatheter or surgical treatment of valvular and/or coronary artery disease within 90 days prior to randomization COPD with home oxygen therapy Estimated or measured systolic PAP >70 mmHg Stroke within 30 days prior to the randomization Inability to provide written informed consent Participation in another cardiovascular trial before reaching the primary endpoint.
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Thomas Pilgrim, Prof. Dr.
Phone
0041316325000
Email
kardio.studien@insel.ch
First Name & Middle Initial & Last Name or Official Title & Degree
Bartowiak Joanna, Dr. med.
Phone
0041316325000
Email
kardio.studien@insel.ch
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Thomas Pilgrim, Prof. Dr.
Organizational Affiliation
Insel Gruppe AG
Official's Role
Principal Investigator
Facility Information:
Facility Name
Insel Gruppe AG, Inselspital Bern
City
Bern
ZIP/Postal Code
3010
Country
Switzerland
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Thomas Pilgrim, Prof
Facility Name
University Hospital Geneva (HUG)
City
Geneva
Country
Switzerland
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Stephane Noble, Prof

12. IPD Sharing Statement

Plan to Share IPD
No
Citations:
PubMed Identifier
27590452
Citation
Shah AM, Solomon SD. Valvular heart disease in older adults: seeking an ounce of prevention. Eur Heart J. 2016 Dec 14;37(47):3523-3524. doi: 10.1093/eurheartj/ehw354. Epub 2016 Sep 1. No abstract available.
Results Reference
background
PubMed Identifier
32646692
Citation
Khan F, Okuno T, Malebranche D, Lanz J, Praz F, Stortecky S, Windecker S, Pilgrim T. Transcatheter Aortic Valve Replacement in Patients With Multivalvular Heart Disease. JACC Cardiovasc Interv. 2020 Jul 13;13(13):1503-1514. doi: 10.1016/j.jcin.2020.03.052.
Results Reference
background
PubMed Identifier
30354497
Citation
Unger P, Pibarot P, Tribouilloy C, Lancellotti P, Maisano F, Iung B, Pierard L; European Society of Cardiology Council on Valvular Heart Disease. Multiple and Mixed Valvular Heart Diseases. Circ Cardiovasc Imaging. 2018 Aug;11(8):e007862. doi: 10.1161/CIRCIMAGING.118.007862. No abstract available.
Results Reference
background

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Early Versus Deferred Aortic Valve Replacement in Patients With Moderate Aortic Stenosis and Mitral Regurgitation

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