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CAN3T - Canadian TAVI Triage Tool

S

Sunnybrook Health Sciences Centre

Status

Not yet enrolling

Conditions

Aortic Stenosis

Treatments

Other: Triage Tool

Study type

Interventional

Funder types

Other

Identifiers

NCT06551610
CTO-4926

Details and patient eligibility

About

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.

Enrollment

5,060 estimated patients

Sex

All

Ages

18+ years old

Volunteers

No Healthy Volunteers

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

Trial design

Primary purpose

Health Services Research

Allocation

Randomized

Interventional model

Sequential Assignment

Masking

None (Open label)

5,060 participants in 2 patient groups

Standard of Care
No Intervention group
Triage tool
Active Comparator group
Treatment:
Other: Triage Tool

Trial contacts and locations

0

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Central trial contact

CAN3T Project Manager

Data sourced from clinicaltrials.gov

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