Structural Mitral Valve Project

Sponsor
Queen's University (Other)
Overall Status
Recruiting
CT.gov ID
NCT05678868
Collaborator
AFP Innovation Fund (Other)
30
1
36
0.8

Study Details

Study Description

Brief Summary

This is a prospective Quality Improvement (QI) study using the Model for Improvement framework.

The objective of this study is to implement a structured, comprehensive, innovative, and sustainable approach to the management of patients with advanced mitral valve (MV) disease and heart failure (HF) in Southeastern Ontario and to improve healthcare delivery, patient care, and patient outcomes in the context of structural surgical and percutaneous MV interventions. This will be achieved through the strategic implementation, promotion, and evaluation of:

i.The first local Southeastern Ontario Structural Mitral Valve Clinic using an Interdisciplinary heart team (IHT) at the Kingston Health Sciences Centre (KHSC) and its integration with the KHSC's existing Heart Failure Clinic; ii.The first provincial Structural Mitral Valve Clinic electronic referral service on the Ontario electronic services platform; and iii.The promotion of the above through targeted KT (Knowledge Transfer) outreach activities.

Patients for this study will be recruited through medical referral within the south eastern Ontario, Canada region.

Condition or Disease Intervention/Treatment Phase
  • Procedure: MitraClip procedure

Study Design

Study Type:
Observational
Anticipated Enrollment :
30 participants
Observational Model:
Cohort
Time Perspective:
Prospective
Official Title:
Implementation of a Structural Mitral Valve Clinic for the Management of Patients With Heart Failure Refractory to Medical Therapy
Actual Study Start Date :
Feb 1, 2022
Anticipated Primary Completion Date :
Jan 31, 2024
Anticipated Study Completion Date :
Jan 31, 2025

Outcome Measures

Primary Outcome Measures

  1. Wait time 1 [At week three following study entry.]

    The time between date referral made and date acknowledged by cardiologist.

  2. Wait time 2 [At week sixteen following study entry.]

    The time from acceptance for a procedure to time of pre-procedure imaging.

  3. Wait time 3 [At week sixteen following study entry.]

    The time from acceptance for a procedure to time of procedure.

Secondary Outcome Measures

  1. Morbidity 1 [At 30 days post procedure.]

    Morbidity = all cause hospitalization and heart failure hospitalization post procedure.

  2. Morbidity 2 [At one year post procedure.]

    Morbidity = all cause hospitalization and heart failure hospitalization post procedure.

  3. Mortality 1 [At 30 days post procedure.]

    Mortality = all cause mortality

  4. Mortality 2 [At one year post procedure.]

    Mortality = all cause mortality

Other Outcome Measures

  1. Electronic referral patient experience survey [At day one (study entry).]

    A survey of patient experience and satisfaction with the electronic referral method. Comments: The survey will be developed by the study investigator and each patient experience related question will be answered using the following scale: Strongly agree ☐ Agree ☐ Neither agree or disagree ☐ Disagree ☐ Strongly disagree. ☐ NA

  2. Electronic referral usage - eReferrals answered [At day one (study entry).]

    Proportion (%) of eReferral answered

  3. Electronic referral usage - response time [At day one (study entry).]

    median specialist response interval time (days).

  4. Electronic referral usage - inappropriate eReferrals [At day one (study entry).]

    proportion (%) of inappropriate eReferrals.

  5. Electronic referral usage - specialist time [At day one (study entry).]

    median time (hours) spent by specialist on eReferral.

  6. Cost comparison 1 [At one day post procedure.]

    Cost comparison between eReferral and traditional referrals based on number of baseline (pre-procedural) lab tests and investigations.

  7. Cost comparison 2 [On the day prior to procedure.]

    Cost comparison between eReferral and traditional referrals based on number of missed clinic visits.

Eligibility Criteria

Criteria

Ages Eligible for Study:
18 Years and Older
Sexes Eligible for Study:
All
Inclusion Criteria:

All adults (≥18 years of age) patients with primary and secondary moderate to severe MR with HF (preserved or reduced ejection fraction with New York Heart Association (NYHA) Class >II), who have had at least one previous hospitalization for HR, require specialist advisement, and have provided signed informed consent.

Exclusion Criteria:
  • Those who are not eligible for either an MV surgical intervention or a TMVI procedure.

  • Females of childbearing age who are not willing or unable to use a reliable method of birth control.

  • Inpatient referrals.

Contacts and Locations

Locations

Site City State Country Postal Code
1 Kingston Health Sciences Centre Kingston Ontario Canada K7L 2V7

Sponsors and Collaborators

  • Queen's University
  • AFP Innovation Fund

Investigators

None specified.

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.
Responsible Party:
Wael Abuzeid, MD, MSc, Interventional Cardiologist, Assistant Professor, Department of Medicine, Queen's University
ClinicalTrials.gov Identifier:
NCT05678868
Other Study ID Numbers:
  • Version Date January 25, 2022
First Posted:
Jan 10, 2023
Last Update Posted:
Jan 10, 2023
Last Verified:
Dec 1, 2022
Studies a U.S. FDA-regulated Drug Product:
No
Studies a U.S. FDA-regulated Device Product:
No
Additional relevant MeSH terms:

Study Results

No Results Posted as of Jan 10, 2023