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Clinical Trials/NCT07034157
NCT07034157RecruitingNot Applicable

A Real-World Study on Ultrasound-Based Screening and Integrated Therapeutic Strategies for Patients With Concomitant Coronary and Cervicocephalic Artery Stenosis

Beijing Anzhen Hospital1 site in 1 country1,000 target enrollmentStarted: June 9, 2025Last updated:
Conditions

Trial Snapshot

Phase
Not Applicable
Status
Recruiting
Sponsor
Enrollment
1,000
Locations
1
Primary Endpoint
Prevalence of Head and Neck Artery Stenosis in Patients with Coronary Artery Disease

Study Overview

Brief Summary

This prospective observational cohort study aims to investigate the prevalence and clinical significance of head and neck arterial stenosis in patients with coronary artery disease (CAD) undergoing or scheduled for percutaneous coronary intervention (PCI). Using Doppler ultrasound as the primary screening tool, the study will assess the degree of stenosis and evaluate the impact of different combined treatment strategies on patient outcomes. The research will provide real-world evidence to optimize integrated care approaches for patients with comorbid cardiovascular and cerebrovascular diseases.

Study Design

Study Type
Observational
Observational Model
Cohort
Time Perspective
Prospective

Eligibility Criteria

Ages
18 Years to — (Adult, Older Adult)
Sex
All
Accepts Healthy Volunteers
No

Inclusion Criteria

  • •Age ≥18 years;
  • •Patients with coronary artery disease scheduled to undergo elective percutaneous coronary intervention (PCI) on the following day.

Exclusion Criteria

  • •The expected survival is less than 1 years;
  • •Simultaneously merge other serious diseases;

Outcomes

Primary Outcomes

Prevalence of Head and Neck Artery Stenosis in Patients with Coronary Artery Disease

Time Frame: At baseline (prior to or during initial hospitalization)

The proportion of patients with coronary artery disease who are found to have head and neck artery (e.g., carotid or vertebral artery) stenosis, as determined by duplex ultrasound or other imaging modalities.

Secondary Outcomes

  • mRS Score(365±30 days)
  • mRS score(7±1 days or the day discharged)
  • Rate of cardiovascular and cerebrovascular events(365±30 days)
  • Short-term complications(90±7 days)
  • Long-term complications(365±30 days)

Investigators

Sponsor
Beijing Anzhen Hospital
Sponsor Class
Other
Responsible Party
Principal Investigator
Principal Investigator

Xiaochuan Huo

Prof

Beijing Anzhen Hospital

Study Sites (1)

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