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NCT06816888Active, not recruiting

Impact of Automatic Prompts in Echocardiographic Reports on Referral to Cardiology

Impact of Automatic Prompts in Echocardiographic Reports on Referral to Cardiology - A Randomized Control Study

Source: ClinicalTrials.gov · Last updated 30 Apr 2026

Brief summary (registry, in English)

Echo Prompts study is a multi-center randomized controlled study to evaluate the impact of automatic prompts added to the conclusion of the echocardiographic reports of patient diagnosed with significant VHD 1) suggesting referral to a cardiologist or 2) suggesting referral to a cardiologist and offering the help of the University of Ottawa Heart Institute Center for Valvular Heart Diseases, compared to current standard of care (no prompts) on the rates and time to an evaluation by a cardiologist. We plan to involve a total of 300 patients in total. Primary endpoint will be the rate of referrals of patients having VHD to a cardiologist within 6 months after their TTE.

Status (registry)
Active, not recruiting
Study type
Interventional
Enrollment
300 (actual)
First submitted
29 Jan 2025
Start date
30 Jan 2025
Primary completion date
1 Dec 2026
Lead sponsor
Ottawa Heart Institute Research Corporation
NCT number
NCT06816888

What you commit to

  • Study type: Interventional
  • Participants enrolled: 300
  • From 30 Jan 2025 to the primary completion date, 1 Dec 2026
  • 1 site in 1 country
  • Visits and tests: ask the trial team, the registry does not list them

Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.

Who cannot take part

Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.

Other

  • Patients followed by a cardiologist or referred for a TTE by a Cardiologist
  • Less than moderate AS and MR

Who the study is looking for

  • Consent provided
  • Patients diagnosed with moderate or severe aortic stenosis (AS) (mean pressure gradient ≥ 20 mm Hg or aortic valve area ≤ 1.5 cm2) or mitral regurgitation (MR) (based on integrative approach)
  • Patients referred by a non-cardiologist physician
  • Patients not currently followed by a cardiologist or who have seen a cardiologist within 24 months prior to the TTE

Age in the registry: 18 years to - · Sex: All · Does not accept healthy volunteers

Full criteria on ClinicalTrials.gov

Sites (1)

Sites in registry order. Pick your city on the disease page to sort them by distance.

SiteCityCountrySite status
University of Ottawa Heart Institute
Coordinator of this site? Confirm its status
OttawaCanadaUnknown status

This page is information, not medical advice. Discuss any trial with your doctor.