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Evidence-Based Practice and Cost-Effectiveness Analysis of a Hypertension-Certified Center Management Model for Shortening Time-to-Target Blood Pressure in Young and Middle-Aged Hypertensive Patients

Evidence-Based Practice and Cost-Effectiveness Analysis of a Hypertension-Certified Center Management Model for Shortening Time-to-Target Blood Pressure in Young and Middle-Aged Hypertensive Patients

Status
Recruiting
Phases
Unknown
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2500111802
Enrollment
Unknown
Registered
2025-11-06
Start date
2025-07-22
Completion date
Unknown
Last updated
2025-11-11

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Essential hypertension

Interventions

Observation Group of Primary hypertension:None

Sponsors

Peking University Shenzhen Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
35 Years to 65 Years

Inclusion criteria

Inclusion criteria: 1. Those aged 35 to 65 years old; 2. Patients diagnosed with essential hypertension, including those who are newly diagnosed with hypertension or are currently undergoing antihypertensive treatment; 3. Informed consent and voluntary participation in research.

Exclusion criteria

Exclusion criteria: 1.SBP>=190mmHg; 2. Those who have persistent atrial fibrillation or arrhythmia that affects the measurement of electronic blood pressure monitors; 3. Patients with combined cardiomyopathy (including hypertrophic cardiomyopathy and dilated cardiomyopathy), rheumatic heart disease, congenital heart disease, and severe valvular heart disease who need to undergo valve replacement during the study period; 4. Those with NYHA grade III or IV heart failure at the time of screening, or those who have been hospitalized due to the aggravation of chronic heart failure in the past 6 months; 5. Severe liver or kidney disease (alanine aminotransferase >= three times the upper limit of normal;) 6. Patients undergoing dialysis treatment or with an estimated glomerular filtration rate of less than 30ml/min/1.73m^2, or with a serum creatinine level greater than 2.5mg/dL[>221umol/L]; 7. Those with cognitive impairment, confusion or language communication disorders; 9. Those who are unable to upload blood pressure information or have no one to assist in uploading blood pressure information.

Design outcomes

Primary

MeasureTime frame
The proportion of time taken to reach the target systolic blood pressure (110<=SBP<130 mmHg);

Countries

China

Contacts

Public ContactQuan Shuping

Peking University Shenzhen Hospital

quanshupingqq@163.com+86 755 8392 3333

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 4, 2026