CAN3T - Canadian TAVI Triage Tool
Not Applicable
Not yet recruiting
- Conditions
- Aortic Stenosis
- Interventions
- Other: Triage Tool
- Registration Number
- NCT06551610
- Lead Sponsor
- Sunnybrook Health Sciences Centre
- Brief Summary
The goal of this trial is to see if a tool that may reduce wait times will reduce bad outcomes in participants on the TAVI waitlist. The main questions it aims to answer are:
* How many deaths, hospitalizations, or urgent TAVI procedures take place while participants wait
* Days alive and out of hospital at 30 days and 12 weeks, total health care costs, and wait times
Researchers will compare usual wait times to see if the tool reduces death, hospitalizations, and urgent procedures.
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- NOT_YET_RECRUITING
- Sex
- All
- Target Recruitment
- 5060
Inclusion Criteria
- All patients referred for TAVI who are 18 years or older at one of 11 TAVI hospitals
Exclusion Criteria
- Any inpatient referrals who have an urgent inpatient TAVI on the same admission
- Any referral during the 1-month transition period
Study & Design
- Study Type
- INTERVENTIONAL
- Study Design
- SEQUENTIAL
- Arm && Interventions
Group Intervention Description Triage tool Triage Tool -
- Primary Outcome Measures
Name Time Method To assess the efficacy of using the CAN3T tool in triage compared to standard care, in TAVI patients, including: reduce wait-time adverse events, improve patient-centred outcomes, and reduce wait-time health care utilization. From the beginning of enrollment and continuing for 32 months. Composite of death, all-cause hospitalization or urgent TAVI (in-hospital and unplanned TAVI) on the TAVI waitlist. The waitlist period is defined as period between TAVI referral and first of either death, TAVI procedure or off list.
- Secondary Outcome Measures
Name Time Method