About this trial
The aim of this study was to establish a registration and monitoring system for hypertension in Xinjiang from 2020 to 2030 to obtain real information about patient basic information, patient characteristics, diagnostic test patterns, treatment options, and hospitalization outcomes (including mortality). Treatment complications, hospitalization costs, and end-of-life events (death, major adverse cardiac events, mild adverse cardiovascular events) in patients with hypertension in Xinjiang; and scientific prevention strategies aimed at effectively preventing the onset of hypertension; Guidelines in clinical practice recommend, analyze and develop effective treatment strategies to optimize management and outcomes for patients with hypertension; and create cost-effective assessment systems.
Eligibility criteria
This trial does not accept healthy volunteersQualifiers
A patient diagnosed with primary hypertension who was admitted to the First Affiliated Hospital of Xinjiang Medical University
Disqualifiers
Patients with secondary hypertension, patients with liver and kidney dysfunction,
patients with mental disorders, and patients who are unwilling to participate in this trial
Trial population
A patient diagnosed with primary hypertension who was admitted to the First Affiliated Hospital of Xinjiang Medical University
Trial design
Cohort
Retrospective
Treatments tested in this trial
Standard therapy
Other interventionIndividualized blood pressure reduction program
Treatment groups
Trial outcomes
Primary outcomes
Resistant hypertension
Death (all-cause mortality, mortality from hypertension complications)
Secondary outcomes
Major adverse cardiovascular events
Sponsors and contacts
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