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Clinical Trial Details — Status: Recruiting

Administrative data

NCT number NCT05656820
Other study ID # GSKY20220407
Secondary ID
Status Recruiting
Phase
First received
Last updated
Start date July 1, 2022
Est. completion date December 31, 2023

Study information

Verified date November 2023
Source Suzhou Municipal Hospital
Contact Ya Yang
Phone +86 18911662958
Email echoyangya99@163.com
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

The Chinese Bicuspid Aortic Valve (BAV) Ultrasound imaging cohort study is a Chinese BAV ultrasound imaging cohort study. At present, a retrospective study cohort involving more than 30 hospitals has been established. The prospective multi-center study of BAV is expected to include and follow up 200 outpatients and inpatients with BAV. The clinical, ultrasound imaging and treatment parameters of the patients are collected and the patients are followed up for 2 years. To analyze the prognostic characteristics of BAV patients and establish a Chinese BAV database. The primary endpoint was all-cause death, and the secondary endpoints were heart failure, angina, severe aortic stenosis, severe aortic insufficiency, ascending aortic diameter ≥50mm, and surgery (surgical and interventional). According to the different pathological types of aortic valve in different types of BAV, ultrasound imaging was used to evaluate the different forms of valvular leaflet lesions and prognosis. Finally, it provides a basis for the prognosis, treatment method, treatment timing and treatment plan selection of BAV patients, and lays a foundation for the mechanism study of BAV arterial lesions and the establishment of risk model for the prognosis of BAV patients.


Recruitment information / eligibility

Status Recruiting
Enrollment 200
Est. completion date December 31, 2023
Est. primary completion date December 30, 2023
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group N/A and older
Eligibility Inclusion Criteria: - Ultrasound or other imaging tests to diagnose patients with BAV Exclusion Criteria: - Patients with TAV or/and have significant aortic valve calcification - Those deemed unsuitable for enrollment by clinicians (e.g., end-stage patients, mentally ill patients, non-cooperating patients, etc.) - Those who do not agree to be included

Study Design


Locations

Country Name City State
China Suzhou Municipal Hospital Suzhou

Sponsors (1)

Lead Sponsor Collaborator
Suzhou Municipal Hospital

Country where clinical trial is conducted

China, 

Outcome

Type Measure Description Time frame Safety issue
Primary Diameter of ascending aorta Diameter of ascending aorta shall be taken using leading edge-to-leading edge convention at end diastole. baseline; once a year; through study completion.
See also
  Status Clinical Trial Phase
Active, not recruiting NCT01980797 - International Bicuspid Aortic Valve Consortium (BAVCon)