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Clinical Trial Details — Status: Recruiting

Administrative data

NCT number NCT04212468
Other study ID # 2018300H(R1)
Secondary ID
Status Recruiting
Phase
First received
Last updated
Start date January 1, 2020
Est. completion date December 31, 2050

Study information

Verified date December 2019
Source Guangdong Provincial People's Hospital
Contact Feng Ying-qing, PhD
Phone +862083827812
Email 651792209@qq.com
Is FDA regulated No
Health authority
Study type Observational [Patient Registry]

Clinical Trial Summary

China is entering an aging society. As the number of elderly population continues to increase, the elderly are facing many social problems that deserve the attention of all sectors of society. Hypertension is one of the common diseases in the elderly population. Hypertension is the most common chronic diseases and a most important risk factor for cardiovascular and cerebrovascular diseases, and also a substantial public health problem. Home blood pressure monitoring is simple, not only can find hypertension, but also can guide the treatment of patients with hypertension. The purpose of the study is to investigate the association between home blood pressure and adverse outcomes in community elderly population.


Description:

Study population includes subjects who living in community, of any race or ethnicity, 65 or older years of age, and have provided written informed consent to provide home blood pressure monitoring at one or more study visits.

Physical examination, questionnaire survey and biological sample collection will be conducted at baseline and the incidence of a composite of major adverse cardiovascular events will be investigated during follow-up.


Recruitment information / eligibility

Status Recruiting
Enrollment 6000
Est. completion date December 31, 2050
Est. primary completion date December 31, 2024
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group 65 Years and older
Eligibility Inclusion Criteria:

•=65 years old

- Signed informed consent

- Life expectancy is greater than 1 year

Exclusion Criteria:

- <65 years old

- Unsigned informed consent

Study Design


Related Conditions & MeSH terms


Intervention

Other:
no intervention
no intervention

Locations

Country Name City State
China Feng Yingqing Guangzhou Guangdong
China Guangdong Provincial People's Hospital Guangzhou Guangdong

Sponsors (1)

Lead Sponsor Collaborator
Guangdong Provincial People's Hospital

Country where clinical trial is conducted

China, 

Outcome

Type Measure Description Time frame Safety issue
Other Number of participants with reported hospitalization due to other diseases The incidence rate of tumor, fracture, cataract etc. From date of inclusion until the date of first event, assessed up to 1 year
Primary All-Cause Mortality All-cause mortality was confirmed through a combination of hospital medical records, telephone contacts with patients or family members, and death registration at the Center for Disease Control and Prevention. From date of inclusion until the date of death from any cause, assessed up to 1 year
Primary Cardiovascular Mortality Cardiovascular mortality was defined as death attributable to an ischemic cardiovascular cause (including fatal cardiovascular events and stroke). From date of inclusion until the date of death from any cause, assessed up to 1 year
Secondary Secondary outcomes of cardiovascular diseases The number of and the incidence rate of cardiovascular diseases. Through study completion, an average of 1 years
Secondary Secondary outcomes of cerebrovascular diseases The incidence rate of cerebrovascular diseases. Through study completion, an average of 1 years
Secondary Secondary outcomes of kidney The incidence rate of renal injure and end-stage renal disease Through study completion, an average of 1 years
Secondary Secondary outcomes of hypertension The incidence rate of hypertension Through study completion, an average of 1 years
Secondary Secondary outcomes of diabetes The incidence rate of diabetes Through study completion, an average of 1 years
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