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Clinical Trials in China / NCT06160921
Recruiting Observational

Prognostic Model of Hypertension

NCT06160921 · tracked via the Priya Life Science China tracker
Sponsor
Xinjiang Medical University
Phase
Observational
Started
2020-01-01
Last updated
2024-03-28

Condition(s) studied

Hypertension

Investigational drug(s) / intervention(s)

Standard therapy

Standard therapy: Individualized blood pressure reduction program

Study summary

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

Sex
ALL
Min age
Max age
Healthy volunteers
No
Inclusion Criteria: * A patient diagnosed with primary hypertension who was admitted to the First Affiliated Hospital of Xinjiang Medical University Exclusion Criteria: * Patients with secondary hypertension, patients with liver and kidney dysfunction, * patients with mental disorders, and patients who are unwilling to participate in this trial

Primary outcome measure(s)

Trial sites (1)

FacilityCityRegionStatus
The First Affiliated Hospital of Xinjiang Medicial University Ürümqi Xinjiang Recruiting

More Xinjiang Medical University trials in China

Other trials for the same condition

Official registry record

This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View NCT06160921 on ClinicalTrials.gov ↗ ← All trials in China