TTE Improves Clinical Management of Stable Chest Pain
TICM-SCP
Improving the Clinical Management of Stable Chest Pain Based on Imaging: a Registry of Transthorcic Echocardiography
1 other identifier
observational
50,000
1 country
1
Brief Summary
The investigator aims to prospectively enroll patients who were referred for transthorcic echocardiography (TTE) for the assessment of stable chest pain (SCP) suspected of obstructive coronary artery disease (CAD). All patients underwent TTE according to established guidelines and local institutional protocols. This study will determine if TTE-based imaging evaluation can provide more informaton to improve clinical management for SCP, including fewer MACE and better decision-making of downstream investigations and therapeutic interventions.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P75+ for all trials
Started Jan 2025
Longer than P75 for all trials
1 active site
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
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Study Timeline
Key milestones and dates
Study Start
First participant enrolled
January 1, 2025
CompletedFirst Submitted
Initial submission to the registry
July 3, 2025
CompletedFirst Posted
Study publicly available on registry
July 14, 2025
CompletedPrimary Completion
Last participant's last visit for primary outcome
December 31, 2030
ExpectedStudy Completion
Last participant's last visit for all outcomes
December 31, 2040
July 18, 2025
July 1, 2025
6 years
July 3, 2025
July 15, 2025
Conditions
Outcome Measures
Primary Outcomes (1)
Major adverse cardiovascular events
10 years
Secondary Outcomes (3)
Invasive coronary angiography
10 years
Medication prescription
10 years
Coronary revascularization
10 years
Study Arms (1)
TTE
Interventions
All patients underwent TTE according to established guidelines and local institutional protocols. The imaging data were evaluated using different image post-processing software to comprehensively analyse anatomical, functional and histological information of coronary.
Eligibility Criteria
Patients who were referred for TTE for the assessment of SCP suspected of CAD.
You may qualify if:
- symptomatic patients with SCP suspected of obstructive CAD.
- referred for TTE for the assessment of SCP.
- ≥18 years of age.
- signed informed consent.
You may not qualify if:
- acute coronary syndromes
- previous CAD or coronary revascularization
- nonsinus rhythm
- cardiomyopathy, valvular disease, congenital heart disease or left cardiac insufficiency because of other reasons
Contact the study team to confirm eligibility.
Sponsors & Collaborators
Study Sites (1)
Tianjin Chest Hospital
Tianjin, China
MeSH Terms
Conditions
Condition Hierarchy (Ancestors)
Central Study Contacts
Study Design
- Study Type
- observational
- Observational Model
- COHORT
- Time Perspective
- PROSPECTIVE
- Target Duration
- 10 Years
- Sponsor Type
- OTHER
- Responsible Party
- PRINCIPAL INVESTIGATOR
- PI Title
- Principal Investigator
Study Record Dates
First Submitted
July 3, 2025
First Posted
July 14, 2025
Study Start
January 1, 2025
Primary Completion (Estimated)
December 31, 2030
Study Completion (Estimated)
December 31, 2040
Last Updated
July 18, 2025
Record last verified: 2025-07