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RecruitingNCT06917586MMVUpdated Feb 20, 2026

Mosaic Mitral Valve: Long-Term Outcomes in Patients Under 65

An observational study in Valve Disease, Heart, Valve Replacement and Valve Regurgitation, Mitral, sponsored by Michael Moront. Recruiting at 1 site in United States. Open to participants aged 18 Years to 65 Years. Per ClinicalTrials.gov, last updated 2026-02-20.

Sponsored by Michael Moront · Observational

From the registry’s dates

  • Primary completion was expected by Jul 2026, 3 months ago, but the record still lists the study as recruiting.
  • Started Jan 2025; still recruiting 1 year 9 months later.
Study type
Observational
Model
Cohort
Time perspective
Retrospective
Enrollment
300
Ages
18 Years to 65 Years
Sex
All
01

Study summary

The safety and efficacy of the Mosaic bioprosthetic heart valves for cardiac valve replacement in the aortic position has been well documented throughout the literature. However, few studies assessing structural valve deficiency, patient outcomes and overall product performance in patients under the age of 65 exists for the Mosaic mitral valve bioprosthetic. This study aims to assess valve efficacy, stability, and post operative outcomes in patients who have received the Mosaic mitral valve prothesis at ProMedica Toledo Hospital and were under the age of 65.

Read the detailed description

Background:

Within the U.S., the prevalence of valvular heart disease is estimated at 2.5% with an abrupt increase after the age of 65 years, predominantly due to degenerative etiologies. In patients with significant valve insufficiency or stenosis where repair or reconstruction is not feasible, valve replacement is the most offered solution. The two types of heart valves offered to patients include mechanical or bioprosthetic. The major advantage of bioprosthetic heart valves in comparison to mechanical valves is the lack of post-operative anticoagulant therapy. However, the major disadvantage of bioprosthetic heart valves lie in their reduced durability compared to mechanical valves, with reoperation rates of \~10% at 10 years and up to 30% at 15 years.

The use of porcine bioprosthetic heart valves for cardiac valve replacement first appeared in the late 1960s and have been widely used since due to the avoidance of anticoagulant therapy. One of the major drawbacks associated with bioprosthetic valves is structural valve deterioration (SVD) which can lead to reduced valve durability, necessitating reoperation. The causes of SVD are poorly understood, however, it is thought to result from the accumulation of calcium and lipids on the valve surface. The Medtronic Mosaic mitral bioprosthetic valve is a 3rd-generation, stented porcine heart valve that was originally approved for clinical use in the U.S. in 2000. These valves are treated with a 0.2% glutaraldehyde solution stabilizing the tissue by cross-linking free lysine residues. In addition, the valve is treated with alpha-amino oleic acid (AOATM) which has been shown to mitigate leaflet calcification in animal studies. Long term clinical safety and efficacy of the Mosaic valve in the aortic position is well documented throughout the literature however, few studies exist detailing performance in the mitral position. Moreover, even fewer studies exist detailing overall valve survival in patients under 65 due to the more common recommendation of the use of mechanical valve replacement in this population. The purpose of this study is to examine long-term outcomes in patients who have received the Mosaic mitral valve bioprosthetic and were under the age of 65 at placement.

Significance:

The investigation of the Medtronic mosaic heart valve in the mitral position will allow for a better assessment of product performance and its impact on patient outcomes. Results can inform physicians on the longevity of the product when used in the mitral position allowing for more accurate prediction of replacement time. In addition, the results may provide further information to the safety and efficacy of placement in the mitral position in patients under the age of 65, a population in which mechanical valves are more prevalent.

02

Conditions studied

  • Valve Disease, Heart
  • Valve Replacement
  • Valve Regurgitation, Mitral
  • Valve Heart Stenosis

Keywords

  • Mitral Valve
  • Bioprosthetic
  • Mosaic
  • Valvulopathy
03

In context

Heart Valve Diseases

535 studies on the registry are indexed under Heart Valve Diseases; 173 are open to participants now.

This study's planned enrollment of 300 is close to the median of 300 across 232 observational studies indexed under Heart Valve Diseases.

Browse Heart Valve Diseases studies →

Lead sponsor

This is the only study on the registry with Michael Moront as lead sponsor.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
18 Years to 65 Years
Sexes eligible
All
Accepts healthy volunteers
No
Sampling method
Non-probability sample

Study population

Study population will include patients who received the mosaic mitral valve bioprosthetic and were between 18-65 years of age at the time of surgery.

Inclusion criteria

  • Received the Mosaic Mitral Valve Bioprosthetic at ProMedica Toledo Hospital
  • Under the age of 65

Exclusion criteria

Exclusion Criteria:

  • Over the age of 65
  • Under the age of 18
  • Surgery performed at institutions outside of ProMedica Toledo Hospital
05

Study design

Observational model
Cohort
Time perspective
Retrospective
Enrollment
300 participants (estimated)
Patient registry
No

Groups and cohorts

  • Mitral Valve Replacement

    Patients who have undergone mitral valve replacement at ProMedica Hospital using the mosaic bioprosthesis and were under the age of 65.

06

What researchers measure

Primary outcomes

  1. Mortality

    Mortality in patients who were under the age of 65 when receiving the mosaic mitral valve bioprosthetic at ProMedica hospital. Patient records will be reviewed to determine mortality rate of patients who were under 65 years of age when receiving the mosaic mitral valve bioprosthetic.

    Time frame: From January 2001 to December 2025

  2. Morbidity

    Post operative morbidity rate for a series of outcomes will be assessed in patients who received the Mosaic mitral valve bioprosthetic over time.

    Time frame: January 2001 - December 2025

Secondary outcomes

  1. Valve Stability

    Assess valve stability in patients who received a mosaic mitral valve bioprosthetic at ProMedica Toledo Hospital. Valve stability will be assessed by reviewing post operative echocardiographic data.

    Time frame: From January 2001 to December 2025

  2. Freedom of Re-operation

    A survival analysis for freedom of reoperation will be assessed for patients who were under 65 at the time of mitral valve replacement.

    Time frame: January 2001 - December 2025

07

Study locations

1 of 1 sites recruiting
  • ProMedica Toledo Hospital
    Toledo, Ohio 43606, United States
    Recruiting
08

References and documents

Individual participant data

Plan to share: No

No publications or documents are linked to this record.

09

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Feb 20, 2026, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
10

Registry details

Key details

Study ID
NCT06917586
Lead sponsor
Michael Moront
Responsible party
Michael Moront (Doctor Of Medicine, ProMedica Health System) — Sponsor-investigator
First posted
Apr 8, 2025
Start date
Jan 1, 2025
Primary completion
Jul 1, 2026 (estimated)
Completion
Jul 1, 2027 (estimated)
Last update
Feb 20, 2026

Study contacts

Dawn Muskiewicz, MS
Contact
dawn.muskiewicz@promedica.org
419-291-7517
Leah Stevenson, MS
Contact
leah.stevenson@promedica.org
419-291-3419
Michael Moront, MD
principal investigator · ProMedica Health System

Oversight

Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

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