- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT05404555
Prognostic Value of Right Ventricular Myocardial Strain in Patients With Acute Myocardial Infarction
June 20, 2022 updated by: Peking University Third Hospital
Prognostic Value of Right Ventricular Myocardial Strain in Patients With Acute Myocardial Infarction With Different Infarction-related Vessels
For a long time, the right ventricle has been the "forgotten chamber", but with the deepening of people's understanding of the disease, right ventricular dysfunction has become an important factor to evaluate the disease progression and late prognosis of patients with AMI.
Right ventricular myocardial strain derived from two-dimensional speckle tracking echocardiography is a new method for early evaluation of regional and global right ventricular systolic function, and its repeatability is much higher than that of LVEF.
Acute inferior myocardial infarction is often caused by occlusion of the proximal middle segment of the right coronary artery.
Many studies have confirmed that RVMS is an independent predictor of poor prognosis in patients with AIMI.
However, 60% of the right ventricular systolic function is contributed by the left ventricle and interventricular septum, and the left anterior descending branch and the left circumflex branch are the main sources of blood supply to the left ventricle and interventricular septum, so in theory, non-RCA occlusion can also lead to varying degrees of right ventricular dysfunction.
However, there are few studies on the role of RVMS in predicting the prognosis of AMI patients caused by non-RCA occlusion.
Therefore, the purpose of this study is to prospectively study the value of dynamic changes of RVMS in predicting the prognosis of patients with acute myocardial infarction with different infarct-related vessels, in order to provide more clinical reference information for the diagnosis and treatment of AMI.
Study Overview
Status
Recruiting
Conditions
Intervention / Treatment
Detailed Description
In this study, 200 patients with acute myocardial infarction treated in Peking University Third Hospital from March 2022 to March 2024 were enrolled in this study.
the parameters of myocardial enzymes, blood lipids and echocardiography were collected at the acute stage, 2 weeks and 6 months after discharge, and were followed up for two year.
The echocardiographic parameters and MACE of patients with acute myocardial infarction with different infarction related vessels were compared.
This shows the significance of right ventricular myocardial strain in predicting the prognosis of patients with acute myocardial infarction.
Study Type
Observational
Enrollment (Anticipated)
200
Contacts and Locations
This section provides the contact details for those conducting the study, and information on where this study is being conducted.
Study Locations
-
-
Beijing
-
Beijing, Beijing, China, 100191
- Recruiting
- Peking University Third Hospital
-
Contact:
- Guisong Wang, doctor
- Phone Number: 13701070359
- Email: guisongwang@bjmu.edu.cn
-
Contact:
- Pengqiang Li, doctor
- Phone Number: 18535915565
- Email: Simon18535915565@163.com
-
-
Participation Criteria
Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.
Eligibility Criteria
Ages Eligible for Study
35 years to 85 years (Adult, Older Adult)
Accepts Healthy Volunteers
No
Genders Eligible for Study
All
Sampling Method
Probability Sample
Study Population
patients with acute myocardial infarction undergoing primary percutaneous coronary intervention are included.
Description
Inclusion Criteria:
- Males and females were between 35 and 85 years old;
- coronary artery disease underwent emergency PCI for NSTEMI or primary PCI for STEMI;
- coronary artery type was right coronary dominance;
- regular follow-up for 2 year.
Exclusion Criteria:
- Patients who cannot complete 2D speckle tracking imaging;
- patients with severe valvular disease, cardiomyopathy, or congenital heart disease; severe liver and kidney insufficiency or chronic respiratory disease;
- previous PCI or CABG;
- coronary artery type: Left crown dominance.
Study Plan
This section provides details of the study plan, including how the study is designed and what the study is measuring.
How is the study designed?
Design Details
- Observational Models: Cohort
- Time Perspectives: Prospective
Cohorts and Interventions
Group / Cohort |
Intervention / Treatment |
|---|---|
|
acute myocardia infarction patients with right coronary artery occlusion
|
Two-dimensional speckle tracking echocardiography is used to assess cardiac function in all enrolled patients
|
|
acute myocardia infarction patients with non-right coronary artery occlusion
|
Two-dimensional speckle tracking echocardiography is used to assess cardiac function in all enrolled patients
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Major Adverse Cardiovascular Events
Time Frame: 2 years
|
Nonfatal stroke, nonfatal myocardial infarction, target vessel requiring revascularization, death
|
2 years
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
Study record dates
These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.
Study Major Dates
Study Start (Actual)
October 1, 2021
Primary Completion (Anticipated)
May 30, 2024
Study Completion (Anticipated)
October 30, 2024
Study Registration Dates
First Submitted
May 31, 2022
First Submitted That Met QC Criteria
May 31, 2022
First Posted (Actual)
June 3, 2022
Study Record Updates
Last Update Posted (Actual)
June 24, 2022
Last Update Submitted That Met QC Criteria
June 20, 2022
Last Verified
March 1, 2022
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- M2022093
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
No
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
No
Studies a U.S. FDA-regulated device product
No
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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