Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
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COMPLETED
366 participants
OBSERVATIONAL
2022-04-01
2022-05-31
Brief Summary
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Detailed Description
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Conditions
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Study Design
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CASE_ONLY
RETROSPECTIVE
Study Groups
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ICU group
patients admitted to ICU with PRES.
Whether the patient needs to be admitted to the ICU
According to ICU admission or not, patients were grouped into ICU group and NOT-ICU group.
Non-ICU group
patients not admitted to ICU with PRES.
Whether the patient needs to be admitted to the ICU
According to ICU admission or not, patients were grouped into ICU group and NOT-ICU group.
Interventions
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Whether the patient needs to be admitted to the ICU
According to ICU admission or not, patients were grouped into ICU group and NOT-ICU group.
Eligibility Criteria
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Inclusion Criteria
2. all patients provided written informed consent
Exclusion Criteria
2. patients combined with mental illness
16 Years
50 Years
FEMALE
No
Sponsors
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Dunjin Chen
OTHER
Responsible Party
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Dunjin Chen
Director of obstetrics
Principal Investigators
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Dunjin Chen
Role: PRINCIPAL_INVESTIGATOR
The Third Affiliated Hospital of Guangzhou Medical University
Locations
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Department of Obstetrics and Gynecology, Key Laboratory for Major Obstetric Diseases of Guangdong Province, The Third Affiliated Hospital of Guangzhou Medical University
Guangzhou, , China
Countries
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Other Identifiers
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2019A151510102
Identifier Type: -
Identifier Source: org_study_id
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