Retrospective Tube Feeding Tolerance in Adults With Intolerance After Switch to a Peptide-Based Formula
NCT ID: NCT03048409
Last Updated: 2019-07-12
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
10 participants
OBSERVATIONAL
2017-07-24
2018-10-02
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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Enteral tube fed adults
Enteral formula
Enteral Formula
Enteral feeding with a peptide-based formula.
Interventions
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Enteral Formula
Enteral feeding with a peptide-based formula.
Eligibility Criteria
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Inclusion Criteria
* Prescribed enteral nutrition with the goal to provide at least 90% of estimated daily calorie and protein requirements for ≥ 2 weeks prior to switch
* Received enteral nutrition with an intact protein formula for a minimum of three days prior to a switch to a peptide-based formula
* Have documentation of intolerance to an intact protein formula, followed by a switch in formula received to a peptide-based formula
* Receiving a peptide-based formula formula for ≥ 2 weeks
* Have documentation of an assessment of feeding tolerance following the switch
* Formulas received must be indicated for use in adults.
Exclusion Criteria
* Having any infection, including upper respiratory, viral, gastroenteritis,wound infections, c difficile, at time of switch
* Having documented cow's milk protein allergy at time of switch
* Medical records lacking information on rationale for switch to a peptide-based formula and/or response to change (positive, neutral or negative).
18 Years
ALL
No
Sponsors
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Société des Produits Nestlé (SPN)
INDUSTRY
Responsible Party
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Principal Investigators
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Jean Chouinard, MD
Role: PRINCIPAL_INVESTIGATOR
St Vincent's Hospital
Locations
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Bruyere Research Institute
Ottawa, Ontario, Canada
Countries
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Other Identifiers
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16.06.US.HCN
Identifier Type: -
Identifier Source: org_study_id
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