Mitral Valve ProlapseNCT03609931
Patient Specific Mitral Valve Modeling for Surgical Planning and Training
An observational study of Mitral Valve Prolapse and Mitral Regurgitation, run by London Health Sciences Centre Research Institute OR Lawson Research Institute of St. Joseph's.
Trial 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. Read more about this study
- Who is it for?
- Ages 18 to 80 years
- Conditions the study is for
- Mitral Valve Prolapse, Mitral Regurgitation, Mitral Valve Disease
- What is being tested?
- Mitral Valve Model
- Type of treatment
- Surgery or procedure
- How many people
- 65 participants
- Where
- No sites listed yet
- Study dates
- Jul 2018to Jan 2020
- Phase
- Observational
- Are there results?
- None posted in the registry
Key requirements
Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.
- Ages 18 to 80 years
- All sexes
- Adult, Older adult
Study population: Adult patients with mitral regurgitation scheduled to undergo mitral valve repair with either a open heart surgical technique or with a MitraClip
Who may be able to join
- Patients undergo mitral valve repair with either surgery of MitraClip techniques
- Over 18 years old
Who cannot join
- Unable to place TEE probe
- Refuse consent
Trial locations and contacts
No sites are listed yet.
About this study
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.
- 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.
Read the 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
- Validate the accuracy of patient specific MV pathologies and repairs in a prospective 65 patient study;
- Optimize our work-flow for creating valve models, in terms of accuracy, manufacture time required, and expense;
- Validate the accuracy of our patient models for both surgical cases and transcatheter MitraClip interventions;
- Being tested
- Mitral Valve Model
- Keywords
- Mitral Valve
- Medical subject headings
- Mitral Valve Prolapse, Mitral Valve Insufficiency
What participants receive
What participants receive. In a randomised study each person is assigned to one group by chance.
Mitral Valve ModelProcedure or surgery
Creation of a mitral valve patient specific model to see if it mimics the patients valve
| Study group | Role | What they receive |
|---|---|---|
| Mitral Valve repair | Patients undergoing mitral valve repair Receives: Procedure: Mitral Valve Model |
What is being measured
The primary outcome is the main question the study is designed to answer.
MR following patient/model repair
The degree and location of residual MR following mitral repair surgery
Measured: Creation and assessment of the model within 1 week before or after surgery/intervention on the patient.
Secondary outcomes (19)
2D measurements of the mitral valve: Anterolateral-Posteromedial Diameter
A 2D measurements taken from the echocardiography images of the mitral valve and model
Measured: Assessment of model within 1 week of surgical or interventional repair on the patient
2D measurements of the mitral valve:Annular Height
A 2D measurements taken from the echocardiography images of the mitral valve and model
Measured: Assessment of model within 1 week of surgical or interventional repair on the patient
2D measurements of the mitral valve: Annular 3D Circumference
A 2D measurements taken from the echocardiography images of the mitral valve and model
Measured: Assessment of model within 1 week of surgical or interventional repair on the patient
2D measurements of the mitral valve:Annular 2D Area
A 2D measurements taken from the echocardiography images of the mitral valve and model
Measured: Assessment of model within 1 week of surgical or interventional repair on the patient
2D measurements of the mitral valve: Annular Ellipticity
A 2D measurements taken from the echocardiography images of the mitral valve and model
Measured: Assessment of model within 1 week of surgical or interventional repair on the patient
2D measurements of the mitral valve: Anterior Leaflet 3D Area
A 2D measurements taken from the echocardiography images of the mitral valve and model
Measured: Assessment of model within 1 week of surgical or interventional repair on the patient
2D measurements of the mitral valve: Posterior Leaflet 3D Area
A 2D measurements taken from the echocardiography images of the mitral valve and model
Measured: Assessment of model within 1 week of surgical or interventional repair on the patient
2D measurements of the mitral valve: Leaflet 3D Area
A 2D measurements taken from the echocardiography images of the mitral valve and model
Measured: Assessment of model within 1 week of surgical or interventional repair on the patient
2D measurements of the mitral valve: Mitral Regurgitation Orifice Area
A 2D measurements taken from the echocardiography images of the mitral valve and model
Measured: Assessment of model within 1 week of surgical or interventional repair on the patient
2D measurements of the mitral valve: Tenting Volume
A 2D measurements taken from the echocardiography images of the mitral valve and model
Measured: Assessment of model within 1 week of surgical or interventional repair on the patient
2D measurements of the mitral valve: Nonplanar Angle
A 2D measurements taken from the echocardiography images of the mitral valve and model
Measured: Assessment of model within 1 week of surgical or interventional repair on the patient
2D measurements of the mitral valve: tenting Height.
A 2D measurements taken from the echocardiography images of the mitral valve and model
Measured: Assessment of model within 1 week of surgical or interventional repair on the patient
ICU LOS
length of stay in the ICU
Measured: Postoperative period until ICU discharge (expected mean of 1 days)]
Hospital LOS
Length of stay in hospital
Measured: Postoperative period until hospital discharge (expected mean of 5 days)
Delirium
Delirium in hospital
Measured: Postoperative period until hospital discharge (expected mean of 5 days)
Renal failure requiring dialysis
Dialysis
Measured: Postoperative period until hospital discharge (expected mean of 5 days)
Stroke,TIA
Diagnosis of stroke
Measured: Postoperative period until hospital discharge (expected mean of 5 days)
Death in Hospital
Death
Measured: Postoperative period until hospital discharge (expected mean of 5 days)
Reoperation for Bleeding
Return to the operating room for re-exploration of the surgical procedure due to excess blood loss in the ICU
Measured: Postoperative period until hospital discharge (expected mean of 5 days)
Timeline
From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.
- First posted1 Aug 2018
- Study startJul 2018 (estimated)
- Primary completionAug 2019 (estimated)
- Study completionJan 2020 (estimated)
Resources
- Official record on ClinicalTrials.govThe registry entry this page is built from, with its full change history.
- Publications (1)Papers the sponsor has linked to this study.
- Other trials for Mitral Valve ProlapseStudies of the same condition, open and under way.
- What the trial phases meanHow a treatment moves from first tests in people to approval.
More details
For doctors and researchers: how the study is designed, who runs it, and its registry IDs.
Study design
- Study type
- Observational
- Observational model
- Case only
- Time perspective
- Prospective
- Enrolment
- 65 participants (estimated)
Sponsor and investigators
- Lead sponsor
- London Health Sciences Centre Research Institute OR Lawson Research Institute of St. Joseph's
- Sponsor type
- University, hospital or other
- Responsible party
- Principal investigator, Daniel Bainbridge, London Health Sciences Centre Research Institute OR Lawson Research Institute of St. Joseph's
IDs, dates and publications
- ClinicalTrials.gov ID
- NCT03609931
- Sponsor's protocol ID
- 111462
- Status last verified
- Jul 2018
- First submitted
- 12 Jun 2018
- Last updated
- 1 Aug 2018
- Results posted
- No
- Data monitoring committee
- No
- FDA-regulated drug
- No
- FDA-regulated device
- No
- Individual data sharing
- No
Publications
Ginty O, Moore J, Peters T, Bainbridge D. Modeling Patient-Specific Deformable Mitral Valves. J Cardiothorac Vasc Anesth. 2018 Jun;32(3):1368-1373. doi: 10.1053/j.jvca.2017.09.005. Epub 2017 Sep 7.
PubMed 29221976
Study at a glance
From the registry record, last updated by the sponsor on 1 Aug 2018. Recruitment status is as the sponsor reported it: confirm with the study team.
- Official title
- Patient Specific Mitral Valve Modeling for Surgical Planning and Training
- ClinicalTrials.gov ID
- NCT03609931
- Acronym / sponsor ID
- 111462
- Keywords
- Mitral Valve
- Study type
- Observational
- Recruitment status
- Unknown status
- Enrolment
- 65 participants (estimated)
- Lead sponsor
- London Health Sciences Centre Research Institute OR Lawson Research Institute of St. Joseph'sUniversity, hospital or other
- Study start
- Jul 2018 (estimated)
- Primary completion
- Aug 2019 (estimated)
- Study completion
- Jan 2020 (estimated)
- First posted
- 1 Aug 2018 (actual)
- Results
- Not posted in the source record
Clinical summary
The research question as the sponsor registered it. This describes what the study plans to test, not what it found.
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.
- 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.
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
- Validate the accuracy of patient specific MV pathologies and repairs in a prospective 65 patient study;
- Optimize our work-flow for creating valve models, in terms of accuracy, manufacture time required, and expense;
- Validate the accuracy of our patient models for both surgical cases and transcatheter MitraClip interventions;
Study design
- Observational model
- Case only
- Time perspective
- Prospective
- Number of arms
- 1
| Arm | Type | Receives |
|---|---|---|
| Mitral Valve repair | – | Procedure: Mitral Valve ModelPatients undergoing mitral valve repair |
Who may qualify
- Ages
- 18 to 80 years
- Sex
- All
- Age groups
- Adult, Older adult
- Study population
- Adult patients with mitral regurgitation scheduled to undergo mitral valve repair with either a open heart surgical technique or with a MitraClip
Key inclusion criteria (2 listed)
- Patients undergo mitral valve repair with either surgery of MitraClip techniques
- Over 18 years old
Key exclusion criteria (2 listed)
- Unable to place TEE probe
- Refuse consent
Eligibility is decided by the study team after screening; this overview does not establish that a patient qualifies. Full inclusion and exclusion criteria.
Interventions
| Intervention | Type | Arms |
|---|---|---|
| Mitral Valve ModelCreation of a mitral valve patient specific model to see if it mimics the patients valve | Procedure or surgery | Mitral Valve repair |
Primary outcome
MR following patient/model repair
Time frame: 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
19 secondary outcomes
2D measurements of the mitral valve: Anterolateral-Posteromedial Diameter
Time frame: Assessment of model within 1 week of surgical or interventional repair on the patient
2D measurements of the mitral valve:Annular Height
Time frame: Assessment of model within 1 week of surgical or interventional repair on the patient
2D measurements of the mitral valve: Annular 3D Circumference
Time frame: Assessment of model within 1 week of surgical or interventional repair on the patient
2D measurements of the mitral valve:Annular 2D Area
Time frame: Assessment of model within 1 week of surgical or interventional repair on the patient
2D measurements of the mitral valve: Annular Ellipticity
Time frame: Assessment of model within 1 week of surgical or interventional repair on the patient
2D measurements of the mitral valve: Anterior Leaflet 3D Area
Time frame: Assessment of model within 1 week of surgical or interventional repair on the patient
2D measurements of the mitral valve: Posterior Leaflet 3D Area
Time frame: Assessment of model within 1 week of surgical or interventional repair on the patient
2D measurements of the mitral valve: Leaflet 3D Area
Time frame: Assessment of model within 1 week of surgical or interventional repair on the patient
2D measurements of the mitral valve: Mitral Regurgitation Orifice Area
Time frame: Assessment of model within 1 week of surgical or interventional repair on the patient
2D measurements of the mitral valve: Tenting Volume
Time frame: Assessment of model within 1 week of surgical or interventional repair on the patient
2D measurements of the mitral valve: Nonplanar Angle
Time frame: Assessment of model within 1 week of surgical or interventional repair on the patient
2D measurements of the mitral valve: tenting Height.
Time frame: Assessment of model within 1 week of surgical or interventional repair on the patient
ICU LOS
Time frame: Postoperative period until ICU discharge (expected mean of 1 days)]
Hospital LOS
Time frame: Postoperative period until hospital discharge (expected mean of 5 days)
Delirium
Time frame: Postoperative period until hospital discharge (expected mean of 5 days)
Renal failure requiring dialysis
Time frame: Postoperative period until hospital discharge (expected mean of 5 days)
Stroke,TIA
Time frame: Postoperative period until hospital discharge (expected mean of 5 days)
Death in Hospital
Time frame: Postoperative period until hospital discharge (expected mean of 5 days)
Reoperation for Bleeding
Time frame: Postoperative period until hospital discharge (expected mean of 5 days)
Results and safety
Results are not available in the source record.
Research links
- Official record on ClinicalTrials.govLast updated by the sponsor 1 Aug 2018.
- Background: PubMed 29221976Ginty O, Moore J, Peters T, Bainbridge D. Modeling Patient-Specific Deformable Mitral Valves. J Cardiothorac Vasc Anesth. 2018 Jun;32(3):1368-1373. doi: 10.1053/j.jvca.2017.09.005. Epub 2017 Sep 7.
- Individual participant dataSharing planned: No
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Referral and contact
AzTrials does not enrol participants or take referrals. Contact the study team or a site listed below; they decide who can take part. This study is not recruiting at the moment.
Questions about this trial
What is this clinical trial studying?
An observational study of Mitral Valve Prolapse and Mitral Regurgitation, run by London Health Sciences Centre Research Institute OR Lawson Research Institute of St. Joseph's.
The full registered description is in the About this study section and the official record.
Who may be eligible to take part?
The sponsor lists 2 inclusion and 2 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.
Is this clinical trial currently recruiting?
The record says: status not confirmed, as of the sponsor's last update on 1 Aug 2018. Status can change between updates, so confirm with the study contact before making plans.
What are the possible benefits and risks?
They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.
Are results available for this study?
Results are not available in the source record.
How can a doctor refer a patient or contact the research team?
Contact Daniel Bainbridge, MD FRCPC (5192004235, daniel.bainbridge@lhsc.on.ca), or a site near the patient. AzTrials does not enrol participants or take referrals.
What does the primary outcome measure?
MR following patient/model repair (time frame: Creation and assessment of the model within 1 week before or after surgery/intervention on the patient.). It is what the study was designed to measure, not a finding.
Where can I read the original study information?
On the ClinicalTrials.gov record for NCT03609931, which also lists 1 linked publication.
Does a listing mean the treatment is approved or proven to work?
No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.
How often is this information updated?
AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 1 Aug 2018.