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Status unknownNCT04015843Updated Nov 25, 2019

Compliance of Blood Pressure and Lipid in Hypertensive Patients Under the Management of Hospitals at Different Levels

An observational study in Hypertension, sponsored by China Cardiovascular Association. Status unknown at 1 site in China. Open to participants aged 18 Years and older. Per ClinicalTrials.gov, last updated 2019-11-25.

Sponsored by China Cardiovascular Association · Observational

The sponsor has not verified this record recently (last verified Jun 2019), so the status shown — last known as Recruiting — may be out of date.
Study type
Observational
Model
Cohort
Time perspective
Prospective
Enrollment
1,800
Ages
18 Years and older
Sex
All
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Study summary

This is a multi-center, prospective cohort study that collects only diagnostic and therapeutic data in subjects but does not interfere with treatment.

Read the detailed description

The study aims to assess blood pressure and lipid levels, the use of lipid-lowering and antihypertensive drugs, and treatment compliance and adverse events in hypertensive outpatients of 30 hospitals of different levels, following them up for 1 and 3 months after treatment, respectively. The study would reveal the compliance of blood pressure and lipid levels in hypertensive patients under management of hospitals at different levels, and analyze factors affecting blood pressure or lipid levels associated with treatment compliance. Therefore, the study would provide clinical data from the real world for future prevention and control of CVD in China.

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Conditions studied

  • Hypertension

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03

In context

Hypertension

6,689 studies on the registry are indexed under Hypertension; 965 are open to participants now.

This study's planned enrollment of 1,800 is above the median of 210 across 1,359 observational studies indexed under Hypertension.

Browse Hypertension studies →

Lead sponsor

China Cardiovascular Association is the lead sponsor of 6 studies on the registry; none are open to participants now.

Counted across the registry records on this site, refreshed daily.

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Who can participate

Ages eligible
18 Years and older
Sexes eligible
All
Accepts healthy volunteers
No
Sampling method
Non-probability sample

Study population

Initial diagnosis of primary hypertension

Inclusion criteria

Patients meeting the following criteria will be included:

  1. Age ≥18 years, male or female;
  2. Agreement for blood pressure and lipid testing;
  3. Initial diagnosis of primary hypertension, with blood pressure conforming to the diagnostic criteria of the 2018 Guidelines for the Prevention and Treatment of Hypertension in China [14] (with no antihypertensive drugs, SBP ≥ 140 mmHg and/or DBP ≥ 90 mmHg after three tests performed on different days); or a history of primary hypertension but incompliant blood pressure;
  4. Willingness to participate in the study and signing of informed consent.

Exclusion criteria

Exclusion Criteria:

  • Patients meeting the following criteria will be excluded:

    1. Involvement in an interventional clinical research;
    2. Pregnancy or lactation in women;
    3. Complication with malignant tumors;
    4. Diagnosis of non-primary hypertension by researchers;
    5. Impaired cognitive ability;
    6. Researchers believing that the patients have other conditions not suitable for the study.
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Study design

Observational model
Cohort
Time perspective
Prospective
Enrollment
1,800 participants (estimated)
Patient registry
No
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What researchers measure

Primary outcomes

  1. The primary endpoint will be compliance of blood pressure in hypertensive patients after 3 months of treatment in hospitals at different levels.

    Blood pressure measurement: Blood pressure in both upper arms will be measured with a sphygmomanometer, with the patient in the sitting position. The mean value of three tests will be used for statistics. When left and right upper arms show different blood pressures, the higher value will be used for statistics.

    Time frame: 3 months

Secondary outcomes

  1. Percentage of outpatients with abnormal blood lipid levels in hospitals at different levels

    On a CardioChek dry-type biochemical analyzer, the levels of total cholesterol (TC), triglyceride (TG), high-density lipoprotein cholesterol (HDL-C) and low-density lipoprotein cholesterol (LDL-C) in fingertip blood samples will be measured after 12-h fasting

    Time frame: 3 months

  2. Achievement rate of blood lipid levels in hypertensive and dyslipidemic patients after 3 months of treatment in hospitals at different levels

    Achievement rate of blood lipid levels in hypertensive and dyslipidemic patients after 3 months of treatment in hospitals at different levels

    Time frame: 3 months

  3. Compliance of patients towards antihypertensive and lipid-lowering treatments in hospitals at different levels

    Compliance of patients towards antihypertensive and lipid-lowering treatments in hospitals at different levels

    Time frame: 3 months

  4. Factors affecting blood pressure and lipid compliance in different hospitals, such as patient adverse events

    Factors affecting blood pressure and lipid compliance in different hospitals, such as patient adverse events

    Time frame: 3 months

  5. Achievement rate of blood pressure in hypertensive patients under different levels of hospital management after 1 month of treatment

    Achievement rate of blood pressure in hypertensive patients under different levels of hospital management after 1 month of treatment

    Time frame: 1 months

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Study locations

1 of 1 sites recruiting
  • Wuhan Asia Heart Hospital
    Wuhan, Hubei, China
    • Hu Daqing, MD · Contact
    Recruiting
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References and documents

Individual participant data

Plan to share: No

No publications or documents are linked to this record.

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Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Nov 25, 2019, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
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Registry details

Key details

Study ID
NCT04015843
Lead sponsor
China Cardiovascular Association
Responsible party
Sponsor
First posted
Jul 11, 2019
Start date
Aug 22, 2019
Primary completion
Aug 30, 2020 (estimated)
Completion
Nov 30, 2020 (estimated)
Last update
Nov 25, 2019

Study contacts

wei ma, doctor
Contact
kmmawei@sina.com
13681050902
jie wang, doctor
Contact
wang_jie116@126.com
010-83572221
yong huo, master
principal investigator · Peking University First Hospital

Oversight

Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

Not currently enrolling

This study is status unknown, as verified in Jun 2019. You cannot join it, but the record below documents what was studied.

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