Patient Specific Mitral Valve Modeling for Surgical Planning and Training

Sponsor
Lawson Health Research Institute (Other)
Overall Status
Unknown status
CT.gov ID
NCT03609931
Collaborator
(none)
65
18

Study Details

Study Description

Brief Summary

Mitral valve disease is a common pathologic problem occurring in approximately 2% of the general population but climbing to 10% in those over the age of 75 in Canada[1]. This project has three primary goals all of which will positively affect cardiac patient care.

  1. Create patient specific MV models for complex repairs that will allow surgeons the opportunity to practice the repair. 2) Potentially predict the outcomes following minimally invasive repair techniques such as transcatheter treatments (e.g., MitraClip). 3) Provide a model to train individuals on mitral valve repair techniques.
Condition or Disease Intervention/Treatment Phase
  • Procedure: Mitral Valve Model

Detailed Description

BACKGROUND Mitral valve disease is a common pathologic problem occurring in approximately 2% of the general population, but climbing to 10% in those over the age of 75 in Canada. Of this group, approximately 20% have a sufficiently severe form of the disease that may require surgical intervention to restore normal valve function and prevent early mortality [4]. Evidence indicates that the surgeon's individual volume of mitral valve repair cases performed is a determinant of not only successful mitral repair rates, but also freedom from reoperation, and patient survival. For patients previously deemed inoperable due to co-morbidities, new techniques to treat mitral valve disease are being developed. However, assessing the optimal approach and the point at which clinical benefit is exceeded by the poor value or futility of the procedure is one of the biggest clinical challenges for physicians.

In the past decade, 3D echocardiography has emerged as a standard of care in diagnostic and interventional imaging for cardiac surgery and cardiology. This, coupled with the emergence of inexpensive 3D printing technology has led researchers and clinicians to explore how improved imaging and additive manufacturing can be used to improve patient outcomes.

In this context, the investigators have completed a proof-of-concept workflow for creating dynamic, patient specific mitral valve models. In concert with a left ventricle simulator 8], these valve models can mimic patient valve pathologies both anatomically and dynamically, as shown in Doppler ultrasound. In a 10 patient retrospective study, the investigators have demonstrated the ability to accurately re-create patient pathology, perform realistic surgical repairs, and assess realistic valve function post repair. The study team's vision is to create a simulator that can be used to assess patient candidacy for percutaneous interventions, assess different repair options for both percutaneous and surgical interventions, and finally use the model as a simulator for competency-based MV interventions.

RATIONALE Based on our successful proof of concept, the goal is to translate this technology to clinical use by validating our valve models. There are two primary long term goals. First, to validate a system for using patient specific MV models to: 1- assess intervention options, and 2: plan repair strategies for improved patient outcomes. Second, by building a database of MV pathologies, create a competency based simulator/trainer to provide surgeons with increased experience in MV repair techniques.

OBJECTIVES

  1. Validate the accuracy of patient specific MV pathologies and repairs in a prospective 65 patient study;

  2. Optimize our work-flow for creating valve models, in terms of accuracy, manufacture time required, and expense;

  3. Validate the accuracy of our patient models for both surgical cases and transcatheter MitraClip interventions;

Study Design

Study Type:
Observational
Anticipated Enrollment :
65 participants
Observational Model:
Case-Only
Time Perspective:
Prospective
Official Title:
Patient Specific Mitral Valve Modeling for Surgical Planning and Training
Anticipated Study Start Date :
Jul 1, 2018
Anticipated Primary Completion Date :
Aug 1, 2019
Anticipated Study Completion Date :
Jan 1, 2020

Arms and Interventions

Arm Intervention/Treatment
Mitral Valve repair

Patients undergoing mitral valve repair

Procedure: Mitral Valve Model
Creation of a mitral valve patient specific model to see if it mimics the patients valve

Outcome Measures

Primary Outcome Measures

  1. MR following patient/model repair [Creation and assessment of the model within 1 week before or after surgery/intervention on the patient.]

    The degree and location of residual MR following mitral repair surgery

Secondary Outcome Measures

  1. 2D measurements of the mitral valve: Anterolateral-Posteromedial Diameter [Assessment of model within 1 week of surgical or interventional repair on the patient]

    A 2D measurements taken from the echocardiography images of the mitral valve and model

  2. 2D measurements of the mitral valve:Annular Height [Assessment of model within 1 week of surgical or interventional repair on the patient]

    A 2D measurements taken from the echocardiography images of the mitral valve and model

  3. 2D measurements of the mitral valve: Annular 3D Circumference [Assessment of model within 1 week of surgical or interventional repair on the patient]

    A 2D measurements taken from the echocardiography images of the mitral valve and model

  4. 2D measurements of the mitral valve:Annular 2D Area [Assessment of model within 1 week of surgical or interventional repair on the patient]

    A 2D measurements taken from the echocardiography images of the mitral valve and model

  5. 2D measurements of the mitral valve: Annular Ellipticity [Assessment of model within 1 week of surgical or interventional repair on the patient]

    A 2D measurements taken from the echocardiography images of the mitral valve and model

  6. 2D measurements of the mitral valve: Anterior Leaflet 3D Area [Assessment of model within 1 week of surgical or interventional repair on the patient]

    A 2D measurements taken from the echocardiography images of the mitral valve and model

  7. 2D measurements of the mitral valve: Posterior Leaflet 3D Area [Assessment of model within 1 week of surgical or interventional repair on the patient]

    A 2D measurements taken from the echocardiography images of the mitral valve and model

  8. 2D measurements of the mitral valve: Leaflet 3D Area [Assessment of model within 1 week of surgical or interventional repair on the patient]

    A 2D measurements taken from the echocardiography images of the mitral valve and model

  9. 2D measurements of the mitral valve: Mitral Regurgitation Orifice Area [Assessment of model within 1 week of surgical or interventional repair on the patient]

    A 2D measurements taken from the echocardiography images of the mitral valve and model

  10. 2D measurements of the mitral valve: Tenting Volume [Assessment of model within 1 week of surgical or interventional repair on the patient]

    A 2D measurements taken from the echocardiography images of the mitral valve and model

  11. 2D measurements of the mitral valve: Nonplanar Angle [Assessment of model within 1 week of surgical or interventional repair on the patient]

    A 2D measurements taken from the echocardiography images of the mitral valve and model

  12. 2D measurements of the mitral valve: tenting Height. [Assessment of model within 1 week of surgical or interventional repair on the patient]

    A 2D measurements taken from the echocardiography images of the mitral valve and model

  13. ICU LOS [Postoperative period until ICU discharge (expected mean of 1 days)]]

    length of stay in the ICU

  14. Hospital LOS [Postoperative period until hospital discharge (expected mean of 5 days)]

    Length of stay in hospital

  15. Delirium [Postoperative period until hospital discharge (expected mean of 5 days)]

    Delirium in hospital

  16. Renal failure requiring dialysis [Postoperative period until hospital discharge (expected mean of 5 days)]

    Dialysis

  17. Stroke,TIA [Postoperative period until hospital discharge (expected mean of 5 days)]

    Diagnosis of stroke

  18. Death in Hospital [Postoperative period until hospital discharge (expected mean of 5 days)]

    Death

  19. Reoperation for Bleeding [Postoperative period until hospital discharge (expected mean of 5 days)]

    Return to the operating room for re-exploration of the surgical procedure due to excess blood loss in the ICU

Eligibility Criteria

Criteria

Ages Eligible for Study:
18 Years to 80 Years
Sexes Eligible for Study:
All
Inclusion Criteria:
  • Patients undergo mitral valve repair with either surgery of MitraClip techniques

  • Over 18 years old

Exclusion Criteria:
  • Unable to place TEE probe

  • Refuse consent

Contacts and Locations

Locations

No locations specified.

Sponsors and Collaborators

  • Lawson Health Research Institute

Investigators

None specified.

Study Documents (Full-Text)

None provided.

More Information

Publications

Responsible Party:
Daniel Bainbridge, Associate Professor, Lawson Health Research Institute
ClinicalTrials.gov Identifier:
NCT03609931
Other Study ID Numbers:
  • 111462
First Posted:
Aug 1, 2018
Last Update Posted:
Aug 1, 2018
Last Verified:
Jul 1, 2018
Individual Participant Data (IPD) Sharing Statement:
No
Plan to Share IPD:
No
Studies a U.S. FDA-regulated Drug Product:
No
Studies a U.S. FDA-regulated Device Product:
No
Keywords provided by Daniel Bainbridge, Associate Professor, Lawson Health Research Institute
Additional relevant MeSH terms:

Study Results

No Results Posted as of Aug 1, 2018