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RecruitingNCT06160921PHOP-HTUpdated Mar 28, 2024

Prognostic Model of Hypertension

An observational study in Hypertension, sponsored by Xinjiang Medical University. Recruiting at 1 site in China. Per ClinicalTrials.gov, last updated 2024-03-28.

Sponsored by Xinjiang Medical University · Observational

From the registry’s dates

  • Started Jan 2020; still recruiting 6 years 9 months later.
Study type
Observational
Model
Cohort
Time perspective
Retrospective
Enrollment
50,000
Sex
All
01

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.

Read the detailed description

The aim of the study is to establish a platform for monitoring, clinical research and translational medicine in Xinjiang, which aims to provide a basis for future quality improvement and research, and to promote efforts to improve the prognosis of patients with hypertension, and to translate research into improved care for patients, thereby reducing Morbidity and mortality associated with hypertension.

02

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 50,000 is above the median of 210 across 1,359 observational studies indexed under Hypertension.

Browse Hypertension studies →

Lead sponsor

Xinjiang Medical University is the lead sponsor of 20 studies on the registry; 11 are open to participants now.

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

04

Who can participate

Ages eligible
Child (0–17), Adult (18–64), Older adult (65+)
Sexes eligible
All
Accepts healthy volunteers
No
Sampling method
Probability sample

Study population

A patient diagnosed with primary hypertension who was admitted to the First Affiliated Hospital of Xinjiang Medical University

Inclusion criteria

  • A patient diagnosed with primary hypertension who was admitted to the First Affiliated Hospital of Xinjiang Medical University

Exclusion criteria

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
05

Study design

Observational model
Cohort
Time perspective
Retrospective
Enrollment
50,000 participants (estimated)
Patient registry
No

Groups and cohorts

  • 2

    Other: Standard therapy

Interventions

  • OtherStandard therapy

    Individualized blood pressure reduction program

06

What researchers measure

Primary outcomes

  1. Resistant hypertension

    Time frame: 10 years of follow-up Resistant hypertension occurred during this period

  2. Death (all-cause mortality, mortality from hypertension complications)

    Time frame: 10 years of follow-up deaths occurred during this period

Secondary outcomes

  1. Major adverse cardiovascular events

    Time frame: 10 years of follow-up deaths occurred during this period

07

Study locations

1 of 1 sites recruiting
  • The First Affiliated Hospital of Xinjiang Medicial University
    Ürümqi, Xinjiang 830000, China
    Recruiting
08

References and documents

Individual participant data

Plan to share: No

No publications or documents are linked to this record.

09

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Mar 28, 2024, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
10

Registry details

Key details

Study ID
NCT06160921
Lead sponsor
Xinjiang Medical University
Responsible party
Xiang Xie (Xiangxie, MD,The First Affiliated Hospital Of XinJiang Medicial University, Xinjiang Medical University) — Principal investigator
First posted
Dec 7, 2023
Start date
Jan 1, 2020
Primary completion
Jan 1, 2030 (estimated)
Completion
Jan 1, 2030 (estimated)
Last update
Mar 28, 2024

Study contacts

Xiang Xie, Phd
Contact
xiangxie999@sina.com
15099169036

Oversight

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

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