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Clinical Trial Details — Status: Recruiting

Administrative data

NCT number NCT03862183
Other study ID # UPPDATE
Secondary ID
Status Recruiting
Phase
First received
Last updated
Start date July 1, 2017
Est. completion date December 30, 2020

Study information

Verified date March 2019
Source Huashan Hospital
Contact xiufang gao, PhD
Phone +86 13788908071
Email sophiakao@126.com
Is FDA regulated No
Health authority
Study type Observational [Patient Registry]

Clinical Trial Summary

To investigate the proportion, medication use and control rate of metabolic abnormalities such as dyslipidemia in outpatients with hypertension in different levels of hospitals in China. To investigate the gap between guidelines and clinical practices, and analyze the cause. we also set up a continuing medical education program to narrow the gap and the effect of the program will be estimated.


Recruitment information / eligibility

Status Recruiting
Enrollment 21000
Est. completion date December 30, 2020
Est. primary completion date December 30, 2020
Accepts healthy volunteers No
Gender All
Age group 18 Years to 85 Years
Eligibility Inclusion Criteria:

1. Outpatients from departments of Cardiology, Endocrinology, Nephrology, Neurology, Geriatrics or General Internal Medicine.

2. Diagnosed as hypertension. Diagnostic criteria: 1)The office BP measured at the day of visit and at least one time before that day were above the cut-off values ( =140 mmHg SBP and/or =90 mmHg DBP); 2)for patients with normal BP at the day of visit, they should have already been given pre-treatment with antihypertensive drugs = 2 weeks.

3. Voluntary participation.

Exclusion Criteria:

1. Patients aged< 18 years old.

2. Patients without a definite diagnosis of hypertension(for instance, if the patient has been taking antihypertensive drugs irregularly, it is difficult to confirm the diagnosis of hypertension).

3. Patients with a definite diagnosis of secondary hypertension.

4. Patients are diagnosed dyslipidemia with clear cause, such as nephrotic syndrome, severe hypothyroidism, terminal stage of malignancy, etc.

5. Patients are diagnosed end-stage renal disease, hemodialysis, and peritoneal dialysis patients.

6. Patients diagnosed with mental abnormalities who are unable to complete the questionnaire.

7. Patients have once participated in this research during this study cycle(to avoid repeated participation).

Study Design


Intervention

Other:
continuing medical education program
educating all the involved doctor the same medical knowledge on hypertension control

Locations

Country Name City State
China Cardiology Department in Huashan Hospital Shanghai Shanghai

Sponsors (1)

Lead Sponsor Collaborator
Huashan Hospital

Country where clinical trial is conducted

China, 

Outcome

Type Measure Description Time frame Safety issue
Primary rate of blood pressure goal achievement systolic blood pressure<140mmHg and diastolic blood pressure<90mmHg 2017-2020
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