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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT04958395
Other study ID # 2014188
Secondary ID
Status Completed
Phase
First received
Last updated
Start date November 1, 2014
Est. completion date October 31, 2015

Study information

Verified date November 2014
Source Peking University Third Hospital
Contact n/a
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

This study clarified the influence of myocardial bridge on coronary hemodynamics by clarifying FFR and d-FFR to guide clinical intervention and treatment.


Description:

Myocardial bridge is a congenital anatomical abnormality, which is generally considered to be a benign change, but individual can cause angina, myocardial infarction and even sudden death. Previously, it was believed that the degree of myocardial ischemia induced by myocardial bridge was related to factors such as the location, length, and systolic stenosis of the myocardial bridge shown by coronary angiography.However, in recent years, more and more evidence has suggested that there is a high degree of mismatch between anatomical stenosis and its function.Studies have shown that FFR and d-FFR can accurately evaluate the functional significance of stenotic lesions.This study intends to enroll patients who underwent coronary angiography due to chest pain and confirmed the left anterior descending artery (LAD) simple myocardial bridge systolic stenosis ≥30%, and the pressure guide wire was used to measure the FFR and d-FFR of the myocardial bridge lesion under static and dobutamine stress.Analyze the relationship between these functional parameters and the anatomical morphological characteristics of the myocardial bridge and other possible clinical influencing factors, and explore the influence of the morphological characteristics of the myocardial bridge on myocardial hemodynamics,so as to clarify the degree of myocardial bridge shown by angiography may induce obvious myocardial ischemia, which requires clinical intensive intervention.


Recruitment information / eligibility

Status Completed
Enrollment 20
Est. completion date October 31, 2015
Est. primary completion date October 31, 2015
Accepts healthy volunteers No
Gender All
Age group 18 Years and older
Eligibility Inclusion Criteria: - Patients with chest pain aged =18 years old, regardless of gender; - Coronary angiography shows a solitary myocardial bridge with systolic diameter stenosis =30% in LAD; - Have the ability to complete an ECG exercise test; - Sign informed consent and are willing to participate in the intended study. Exclusion Criteria: - Patients with acute coronary syndrome; - Coronary angiography shows that the diameter of atherosclerosis in the non-myocardial bridge area of LAD is =30%; - RCA or LCX has severe fixed stenosis, diameter stenosis =70% or FFR<0.75, and no interventional therapy is accepted; - Hypertrophic obstructive cardiomyopathy or more than moderate heart valve disease; - Atrial fibrillation or severe slow or rapid arrhythmia; - Heart failure with NYHA = Grade III; - Uncontrolled hypertension or systolic blood pressure <100mmHg; - Asthma or severe chronic obstructive pulmonary disease; - Severe liver and kidney dysfunction; - Allergic to contrast agents.

Study Design


Related Conditions & MeSH terms


Intervention

Diagnostic Test:
FFR and d-FFR
Measure FFR and d-FFR

Locations

Country Name City State
n/a

Sponsors (1)

Lead Sponsor Collaborator
Peking University Third Hospital

Outcome

Type Measure Description Time frame Safety issue
Primary Morphological index of myocardial bridge The minimum lumen diameter of the target vessel All indicators were completed within 1 week of coronary angiography.
Secondary Exercise electrocardiogram ST segment depression time 72 hours after coronary angiography
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