Actively Recruiting

All Genders
ID04226612

Association of Inpatient Blood Pressure Levels With In-hospital Adverse Events(APPLE Study)

Led by Guangdong Provincial People's Hospital · Updated on 2020-01-13

100000

Participants Needed

1

Research Sites

574 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

This research aims to investigate the connection between blood pressure levels measured during hospital stays and the occurrence of serious adverse events, including death, in patients admitted for various illnesses. The study includes hospitalized individuals of all ages, races, and ethnic backgrounds. The main focus is to understand how inpatient blood pressure relates to all-cause mortality occurring during hospitalization. Participants are observed without receiving experimental treatments since this is an observational study. Researchers collect and analyze blood pressure data recorded while patients are in the hospital. No interventions or medications are administered as part of the study, and the research does not involve comparison groups or treatments. During the hospital stay, patient blood pressure records and clinical outcomes are monitored and reviewed. The primary outcome measure is the incidence of all-cause mortality that occurs while the patient is hospitalized. The study spans a long period, from the year 2000 to 2030, allowing for comprehensive data collection on inpatient blood pressure and related health outcomes.

CONDITIONS

Brief Title

Association of Inpatient Blood Pressure Levels With In-hospital Adverse Events(APPLE Study)

Who Can Participate

All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Inpatient of any age or race
  • Have available blood pressure data
Not Eligible

You will not qualify if you...

  • Not a patient (non-patient)
  • Death occurring outside the hospital
  • Missing blood pressure data

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Your Study Journey

Screening

Duration - 2 to 4 weeks

Participants are screened for eligibility to participate in the trial.

Monitoring

Duration - Duration of hospital stay

Participants who are hospitalized are observed to assess blood pressure levels and in-hospital adverse events.

Continuous monitoring during hospitalization

Trial Site Locations

Total: 1 location

1

Feng Ying-qing

Guangzhou, Guangdong, China, 510080

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Research Team

F

Feng Ying-qing, PhD

How is the study designed?

Study Type

OBSERVATIONAL

Masking

N/A

Allocation

N/A

Model

N/A

Primary Purpose

N/A

Number of Arms

0

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