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
26 participants
OBSERVATIONAL
2011-05-31
2013-12-31
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
PROSPECTIVE
Study Groups
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critically ill obese adults
Age ≥ 18 years, body mass index (BMI) ≥ 30, in intensive care unit (ICU) requiring tube feeding ≥ 3 days
enteral formula
Complete feeding of study enteral formula, route and regime prescribed by the physician.
Interventions
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enteral formula
Complete feeding of study enteral formula, route and regime prescribed by the physician.
Eligibility Criteria
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Inclusion Criteria
* Surgical or Medical intensive care unit (ICU) patient
* Body mass index (BMI) ≥ 30
Exclusion Criteria
* unable to access gastrointestinal (GI) tract for feeding via tube
* other contraindication to tube feeding
* admitted with burns
* severe head trauma
18 Years
ALL
No
Sponsors
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Société des Produits Nestlé (SPN)
INDUSTRY
Responsible Party
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Locations
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University of Kentucky
Lexington, Kentucky, United States
University of Louisville
Louisville, Kentucky, United States
Countries
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Other Identifiers
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10.02.US.CLI
Identifier Type: -
Identifier Source: org_study_id
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