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
2000 participants
OBSERVATIONAL
2016-09-30
2018-09-30
Brief Summary
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Detailed Description
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Conditions
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Study Design
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OTHER
RETROSPECTIVE
Eligibility Criteria
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Inclusion Criteria
* Admitted to the ICU
* Administered at least one dose of enteral formula
Exclusion Criteria
18 Years
ALL
No
Sponsors
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Geisinger Clinic
OTHER
Société des Produits Nestlé (SPN)
INDUSTRY
Responsible Party
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Principal Investigators
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Joseph Layon, MD, FACP
Role: PRINCIPAL_INVESTIGATOR
Geisinger Clinic
Locations
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Geisinger Medical Center
Danville, Pennsylvania, United States
Geisinger Community Medical Center, Scranton, PA
Scranton, Pennsylvania, United States
Geisinger Wyoming Valley Medical Center
Wilkes-Barre, Pennsylvania, United States
Countries
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Other Identifiers
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16.11.CLI
Identifier Type: -
Identifier Source: org_study_id
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