Risk Factors for ARDS in Patients With Acute Necrotizing Pancreatitis
NCT ID: NCT02641964
Last Updated: 2021-01-25
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
350 participants
OBSERVATIONAL
2015-11-30
2021-01-31
Brief Summary
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Detailed Description
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For enrolled patients, general clinical characteristics were collected. Patients were categorized into two groups according to ARDS or non-ARDS, and the differences of these characteristics between two groups were evaluated. Potential risk factors were collected and studied by using multiple logistic regression analysis.
Conditions
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Study Design
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CASE_CONTROL
RETROSPECTIVE
Study Groups
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ARDS group
patients with acute necrotizing pancreatitis complicated by ARDS
No interventions assigned to this group
non-ARDS group
acute necrotizing pancreatitis patients without ARDS
No interventions assigned to this group
Eligibility Criteria
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Inclusion Criteria
Exclusion Criteria
* presence of ARDS before admission to hospitals,
* unable to partner treatment and leaving hospitals,
* transferring to the investigators' hospitals after treatment,
* missing other necessary data,
* pregnancy.
18 Years
ALL
No
Sponsors
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Nanjing Medical University
OTHER
Responsible Party
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Bin He
Emergency department physician
Principal Investigators
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Bin He, Master
Role: STUDY_DIRECTOR
Nanjing Medical University
Other Identifiers
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JSSRMYY-HB-1
Identifier Type: -
Identifier Source: org_study_id
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