Status:
UNKNOWN
Effects of Intensive Systolic Blood Pressure Lowering Treatment on Out-of-office Blood Pressure - an Ancillary Study to Effects of Intensive Systolic Blood Pressure Lowering Treatment in Reducing RIsk of Vascular evenTs (ESPRIT) Study
Lead Sponsor:
China National Center for Cardiovascular Diseases
Collaborating Sponsors:
Chinese Academy of Medical Sciences, Fuwai Hospital
Conditions:
Blood Pressure
Eligibility:
All Genders
50+ years
Phase:
NA
Brief Summary
This study aims to evaluate the effect of intensive treatment (a target clinic based systolic blood pressure(BP) \<120mmHg) on 24-hour ambulatory blood pressure and home blood pressure, as well as the...
Detailed Description
This study aims to evaluate the effect of intensive treatment (a target clinic based systolic BP \<120mmHg) on 24-hour ambulatory blood pressure and home blood pressure, as well as the effect on White...
Eligibility Criteria
Inclusion
- eligible for the follow up of the main study;
- content to participate in the sub-study.
Exclusion
- frequently working during night-time;
- the non - dominant arm could not wear 24-hour ambulatory blood pressure monitoring due to radiation therapy or physical impairment;
- keep engaged in out-door activities of high physical intensity, e.g. farming or porter, etc.;
- life expectancy is less than 1 year; such as diagnosed with heart failure, cancer, or end-stage renal disease;
- the difference of clinical systolic pressure between upper arms was more than 10 mmHg;
- unable to use smart-phone to upload family blood pressure monitoring data.
Key Trial Info
Start Date :
July 18 2022
Trial Type :
INTERVENTIONAL
Allocation :
ESTIMATED
End Date :
September 30 2023
Estimated Enrollment :
710 Patients enrolled
Trial Details
Trial ID
NCT05352633
Start Date
July 18 2022
End Date
September 30 2023
Last Update
June 28 2022
Active Locations (1)
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1
Fuwai Hospital, Chinese Academy of Medical Sciences
Beijing, Beijing Municipality, China, 100037