- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT04573257
Effect of Aterial Stiffness on Myocardial Work in Patients With Hypertension
Relationship Between Arteriosclerosis and Myocardial Work in Hypertensive Patients With Left Ventricular Ejection Fraction Retention
Study Overview
Status
Conditions
Intervention / Treatment
Detailed Description
Study Type
Enrollment (Anticipated)
Contacts and Locations
Study Contact
- Name: QIN DUAN
- Phone Number: 8618623349865
- Email: 570549500@126.com
Study Contact Backup
- Name: QIAN DUAN
- Phone Number: 8613608393056
Study Locations
-
-
-
Chongqing, China, 400000
- Recruiting
- The First Affiliated Hospital of Chongqing Medical University
-
Contact:
- Qin DUAN
- Phone Number: +861862349865
- Email: 570549500@qq.com
-
-
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
Accepts Healthy Volunteers
Genders Eligible for Study
Sampling Method
Study Population
Description
Inclusion Criteria:
Age 18-65 years
The diagnostic criteria of hypertension were blood pressure systolic blood pressure ≥140mmHg and/or diastolic blood pressure ≥90mmHg in the clinic or receiving antihypertensive drug treatment
The normal high-value diagnostic criteria for hypertension were systolic blood pressure 130-139mmhg and or diastolic blood pressure 85-90mmhg in the clinic
LVEF > 50%
Exclusion Criteria:
coronary atherosclerotic heart disease or symptoms of angina
Cardiomyopathy
Valvular heart disease
Diabetes
Atrial fibrillation
Renal function damage
Pregnancy
Secondary hypertension
Chemotherapy for malignant tumors
Study Plan
How is the study designed?
Design Details
Cohorts and Interventions
Group / Cohort |
Intervention / Treatment |
---|---|
normotensive group
The medical history and basic examination and examination information were collected.
Echocardiography including conventional cardiac ultrasound, tissue Doppler and two-dimensional speckle tracking to measure myocardial strain and noninvasive myocardial work were carried out , and the brachial-ankle pulse wave velocity was measured in parallel.
|
Echocardiography(Conventional ultrasonic imaging,tissue Doppler imaging and non invasive myocardial work) and pulse wave velocity measurement
|
Prehypertension group
The medical history and basic examination and examination information were collected.
Echocardiography including conventional cardiac ultrasound, tissue Doppler and two-dimensional speckle tracking to measure myocardial strain and noninvasive myocardial work were carried out , and the brachial-ankle pulse wave velocity was measured in parallel.
|
Echocardiography(Conventional ultrasonic imaging,tissue Doppler imaging and non invasive myocardial work) and pulse wave velocity measurement
|
hypertensive group
The medical history and basic examination and examination information were collected.
Echocardiography including conventional cardiac ultrasound, tissue Doppler and two-dimensional speckle tracking to measure myocardial strain and noninvasive myocardial work were carried out , and the brachial-ankle pulse wave velocity was measured in parallel.
|
Echocardiography(Conventional ultrasonic imaging,tissue Doppler imaging and non invasive myocardial work) and pulse wave velocity measurement
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
myocardial work
Time Frame: 2020.09-2021.01
|
myocardial work measured by non-invasive left ventricular pressure-strain loop(2D speckle tracking echocardiography method by using the GE Vivid E95 ultrasound system )
|
2020.09-2021.01
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
brachial-ankle pulse wave velocity
Time Frame: 2020.09-2021.01
|
brachial-ankle pulse wave velocity measured by OMRON BP-203RPEIII arteriosclerosis detector
|
2020.09-2021.01
|
Collaborators and Investigators
Sponsor
Investigators
- Principal Investigator: QIN DUAN, First Affiliated Hospital of Chongqing Medical University
Study record dates
Study Major Dates
Study Start (ACTUAL)
Primary Completion (ANTICIPATED)
Study Completion (ANTICIPATED)
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
- 20200910
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
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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