Study to Evaluate the Effectiveness of the Device in Detection of Abnormal Findings on Chest X-ray
NCT ID: NCT05614232
Last Updated: 2022-11-14
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
700 participants
OBSERVATIONAL
2020-02-11
2020-07-01
Brief Summary
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Detailed Description
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Conditions
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Study Design
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COHORT
RETROSPECTIVE
Study Groups
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Positive group
chest radiographs with the specific target radiologic findings (Atelectasis, Calcification, Cardiomegaly, Consolidation, Fibrosis, Mediastinal Widening, Nodule/Mass, Pleural Effusion, Pneumoperitoneum, Pneumothorax)
Chest X-ray
Chest radiographs
Negative group
chest radiographs with no target radiologic findings
Chest X-ray
Chest radiographs
Interventions
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Chest X-ray
Chest radiographs
Eligibility Criteria
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Inclusion Criteria
* Conventional PA or AP chest radiographs
* Chest radiographs with confirmed radiology reports
Exclusion Criteria
* Chest radiographs from dual-energy radiography
* Invert-grayscale chest radiographs
14 Years
ALL
Yes
Sponsors
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Lunit Inc.
INDUSTRY
Responsible Party
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Locations
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SMG-SNU Boramae Medical Center
Seoul, , South Korea
Countries
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Other Identifiers
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LUN_CXR_CA_221
Identifier Type: -
Identifier Source: org_study_id
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