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NCT Number: NCT06917586

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

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.

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Key information

Age range

18 year–65 year

Sex eligibility

All sexes

Study type

Observational

Primary location

ProMedica Toledo Hospital

Toledo, Ohio, 43606, United States

Location status: Recruiting

Location contact

Dawn Muskiewicz, MS

CONTACT

[email protected]

419-291-7517

About this study

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.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

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

Exclusion criteria

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

Treatment and study plan

Primary outcomes

  1. Mortality

    Time frame: From January 2001 to December 2025

    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.

  2. Morbidity

    Time frame: January 2001 - December 2025

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

Secondary outcomes

  1. Valve Stability

    Time frame: From January 2001 to December 2025

    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.

  2. Freedom of Re-operation

    Time frame: January 2001 - December 2025

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

Study contacts

Contact information is provided by the study sponsor or research team.

Dawn Muskiewicz, MS

CONTACT

[email protected]

419-291-7517

Leah Stevenson, MS

CONTACT

[email protected]

419-291-3419

Sponsors and collaborators

Lead sponsor

Michael Moront

Other

Registry information

Official study title

Long Term Patient Outcomes and Product Durability of the Mosaic Mitral Valve Bioprosthesis in Patients Under 65

Acronym: MMV

Important dates

Study start
2025
Primary completion
2026
Study completion
2027
First posted
Apr 8, 2025
Registry last updated
Feb 20, 2026

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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