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
2999 participants
OBSERVATIONAL
2019-10-01
2021-01-31
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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Patients with upper gastrointestinal bleeding
Patients with upper gastrointestinal bleeding undergoing endoscopic procedures at AdventHealth Hospitals in Central Florida
Upper GI Endoscopy
Patients with upper gastrointestinal bleeding undergoing endoscopic therapy. Information regarding the need for interventional radiology procedures or surgical interventions will also be collected in patients in whom endoscopic therapy is not successful.
Interventions
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Upper GI Endoscopy
Patients with upper gastrointestinal bleeding undergoing endoscopic therapy. Information regarding the need for interventional radiology procedures or surgical interventions will also be collected in patients in whom endoscopic therapy is not successful.
Eligibility Criteria
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Inclusion Criteria
* Patient is undergoing endoscopic treatment for upper gastrointestinal bleeding
Exclusion Criteria
* Patient not undergoing endoscopic treatment for upper gastrointestinal bleeding
18 Years
ALL
No
Sponsors
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AdventHealth
OTHER
Responsible Party
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Principal Investigators
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Shyam Varadarajulu, MD
Role: PRINCIPAL_INVESTIGATOR
AdventHealth Orlando
Locations
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Center for Interventional Endoscopy
Orlando, Florida, United States
Countries
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Other Identifiers
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1494617
Identifier Type: -
Identifier Source: org_study_id
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