- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT05638503
Multi-center Study on New Cardiovascular Remodeling and Function Parameters in Hypertension
Study Overview
Status
Conditions
Intervention / Treatment
Detailed Description
Different configurations of hypertension are important risk factor for the morbidity and mortality of cardiovascular and cerebrovascular diseases in China. Studies have shown that left ventricular hypertrophy (LVH) and left atrial enlargement caused by hypertension are independent risk factors for cardiovascular events. The LVM and LAV derived from the normal value data of Chinese healthy adults have been reported to be different from the recommended reference values in guidelines, and the distribution characteristics of hypertension remodeling are also different. However, the characteristics and outcomes of cardiac remodeling in Chinese hypertensive population and whether this difference in configuration has an impact on the treatment, prognosis and cardiovascular events of hypertensive population are still needed to be explored.
This study was to observe the relationship between blood pressure and cardiovascular remodeling evaluated by different standards in hypertensive population, and compare the relationship between different cardiac configurations and cardiovascular events in Chinese hypertensive population.
Twenty research centers and 2200 hypertensions were planned to be collected and followed up in the 12th, 24th, 36th and 48th months after being enrolled in this study. Physical examination, ECG examination, laboratory examination, echocardiography and carotid ultrasound should be taken when baseline and follow-up.
Echocardiographic measurement parameters including M-mode and two-dimensional ultrasonic parameters; doppler ultrasound parameters; relevant parameters of two-dimensional speckle tracking, myocardial work parameters; the left ventricular remodeling parameters (LVM and RWT); cardiac morphological changes; three-dimensional ultrasound parameters were analyzed and the relationship between the echocardiographic measurement parameters and cardiovascular events and prognosis of hypertension.
Study Type
Enrollment (Estimated)
Contacts and Locations
Study Contact
- Name: Yu Zhang, PhD
- Phone Number: +86-18560088296
- Email: zhangyu_505@126.com
Study Contact Backup
- Name: Mei Zhang, PhD
- Phone Number: +86-18560086629
- Email: daixh@vip.sina.com
Study Locations
-
-
Shandong
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Jinan, Shandong, China, 250012
- Recruiting
- Qilu Hospital of Shandong University
-
Contact:
- Lijuan Bu, PhD
- Phone Number: +86-18560088816
- Email: qlyykyc@163.ocm
-
-
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
Accepts Healthy Volunteers
Sampling Method
Study Population
Description
Inclusion Criteria:
- Age 30-75 years old;
- No antihypertensive drugs were used and three blood pressure measurements were conducted on different days, with systolic blood pressure ≥ 140 mmHg (1 mmHg=0.133 kPa) and/or diastolic blood pressure ≥ 90 mmHg; or have a history of hypertension and are using antihypertensive drugs, even if the blood pressure is lower than 140/90 mmHg;
- Left ventricular ejection fraction was normal (LVEF ≥ 0.5).
- All patients agreed to participate in the experiment and signed the informed consent form.
Exclusion Criteria:
- Secondary hypertension caused by renal parenchymal diseases, renal vascular diseases, coarctation of aorta and endocrine system diseases;
- Severe cardiovascular and cerebrovascular diseases; heart valve disease; persistent atrial fibrillation and severe arrhythmia; previously undergone cardiovascular disease surgery;
- Abnormal liver function; abnormal renal function and diabetes;
- Pregnant or breastfeeding women;
- Expected survival time due to non-cardiovascular disease<4 years;
- Patients with poor echocardiographic image quality.
Study Plan
How is the study designed?
Design Details
- Observational Models: Cohort
- Time Perspectives: Prospective
Cohorts and Interventions
Group / Cohort |
Intervention / Treatment |
|---|---|
|
Hypertension with left ventricular hypertrophy group
2015 ASE/EACVI guideline standard: Eccentric hypertrophy, EH: LVMI>115g/ m2(male)or LVMI>95g/ m2(female)and RWT≤0.42 Concentric hypertrophy, CH: LVMI>115g/ m2(male)or LVMI>95g/ m2(female)and RWT>0.42 Reference Values for Chinese (EMINCA) and Configuration Analysis Based on Ganau Typing: Eccentric hypertrophy, EH: LVMI>108g/ m2(male)and RWT≤0.51or LVMI>99g/ m2(female)and RWT≤0.49 Concentric hypertrophy, CH: LVMI>108g/ m2(male)and RWT>0.51 or LVMI>99g/ m2(female)and RWT>0.49 |
Hypertension with normal left ventricular geometry and left ventricular concentric remodeling
|
|
Hypertension with left ventricular non-hypertrophy group
2015 ASE/EACVI guideline standard: Normal left ventricular geometry, NG: LVMI≤115g/m2(male)or LVMI≤95g/m2(female)and RWT≤0.42 Concentric remodeling, CR: LVMI≤115g/m2(male)or LVMI≤95g/ m2(female)and RWT>0.42 Reference Values for Chinese (EMINCA) and Configuration Analysis Based on Ganau Typing: Normal left ventricular geometry, NG: LVMI≤108g/ m2(male)and RWT≤0.51 or LVMI≤99g/ m2(female)and RWT>0.49 Concentric remodeling, CR: LVMI≤108g/ m2(male)and RWT>0.51 or LVMI≤99g/ m2(female)and RWT>0.49 |
Hypertension with left ventricular concentric hypertrophy and left ventricular eccentric hypertrophy
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Emerging atrial fibrillation
Time Frame: Through study completion, on average once a year.
|
The differences in the incidence of atrial fibrillation between the two groups
|
Through study completion, on average once a year.
|
|
Emerging unstable angina, myocardial infarction, heart failure, coronary revascularization, cardiovascular death
Time Frame: Through study completion, on average once a year.
|
The differences in the incidence of unstable angina, myocardial infarction, heart failure, coronary revascularization, cardiovascular death between the two groups
|
Through study completion, on average once a year.
|
|
Emerging transient ischemic attack (TIA) or stroke
Time Frame: Through study completion, on average once a year.
|
The differences in the incidence of transient ischemic attack (TIA) or stroke between the two groups
|
Through study completion, on average once a year.
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Emerging decreased cardiac function with preserved ejection fraction
Time Frame: Through study completion, on average once a year.
|
The differences between the two groups in the incidence of decreased cardiac function with preserved ejection fraction measured by echocardiography compared to that at the baseline
|
Through study completion, on average once a year.
|
|
Emerging cardiac remodeling
Time Frame: Through study completion, on average once a year.
|
The differences between the two groups in the incidence of cardiac remodeling measured by echocardiography compared to that at the baseline
|
Through study completion, on average once a year.
|
|
Emerging aortic aneurysm or aortic dissection
Time Frame: Through study completion, on average once a year.
|
The differences in the incidence of aortic aneurysm or aortic dissection between the two groups
|
Through study completion, on average once a year.
|
|
Emerging serious arrhythmias
Time Frame: Through study completion, on average once a year.
|
ECG showed that QTc (QT interval corrected by heart rate) was more than 500ms or QTc was longer than the baseline level for more than 60ms, emerging torsade de pointes ventricular tachycardia and other serious arrhythmias
|
Through study completion, on average once a year.
|
|
The relationship between the deviations of blood pressure within the same day and the difference of cardiac function indexes
Time Frame: Through study completion, on average once a year.
|
The differences between the two groups in the incidence of the deviations between blood pressure and cardiac function parameters at the same day measured by echocardiography
|
Through study completion, on average once a year.
|
Collaborators and Investigators
Investigators
- Principal Investigator: Mei Zhang, PhD, Qilu Hospital of Shandong University
Study record dates
Study Major Dates
Study Start (Actual)
Primary Completion (Estimated)
Study Completion (Estimated)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Actual)
Study Record Updates
Last Update Posted (Actual)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- QLCR20220272
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
product manufactured in and exported from the U.S.
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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