Recruiting NCT04226612
Association of Inpatient Blood Pressure Levels With In-hospital Adverse Events(APPLE Study)
For patients and families
In plain language
An automatic summary of structured registry data. It is an orientation aid, not a substitute for the official protocol or a physician assessment.
- What is being studied
- This is an observational study: the protocol does not assign a study treatment.
- Who it may be relevant to
- Registry conditions: Blood Pressure. Basic parameters: No limits · All.
- What needs checking
- Age, condition and sex are only basic indicators. Prior treatment, laboratory values and other mandatory requirements appear in the eligibility criteria below.
- Where it takes place
- China
- Next step
- Save the trial, show it to the treating physician, and confirm current recruitment with the study center. Costs, documents and travel →
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Overview
The purpose of the study is to investigate the association between inpatient blood pressure levels and in-hosopital adverse outcomes.
Detailed description
Study population includes subjects who are hospitalized due to illness, of any race or ethnicity, any of age.The primary outcome is all-cause mortality occured in the hospital.
Primary outcome measures
- All-cause mortality [Time frame: during the procedure]
Eligibility criteria
Inclusion criteria
- Inpatient with all age or race;
- Have blood pressure data.
Exclusion criteria
- Non-patients；
- Death outside the hospital；
- Missing blood pressure data.
Criteria are shown verbatim from the registry (in English). Final eligibility is always assessed by the study center.
Study design
- Observational model
- Other
Study locations
China · 1 center
- Feng Ying-qing — Guangzhou
Identifiers
NCT: NCT04226612 · 2018570H(R1)