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

Results pending

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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Recruitment Status

COMPLETED

Total Enrollment

10 participants

Study Classification

OBSERVATIONAL

Study Start Date

2017-07-24

Study Completion Date

2018-10-02

Brief Summary

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A retrospective chart review to assess feeding tolerance in adults who had been switched from an intact protein formula to a peptide-based formula due to feeding intolerance in a complex continuing care facility.

Detailed Description

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Conditions

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Enteral Feeding Intolerance

Study Design

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Observational Model Type

COHORT

Study Time Perspective

RETROSPECTIVE

Study Groups

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Enteral tube fed adults

Enteral formula

Enteral Formula

Intervention Type OTHER

Enteral feeding with a peptide-based formula.

Interventions

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Enteral Formula

Enteral feeding with a peptide-based formula.

Intervention Type OTHER

Eligibility Criteria

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Inclusion Criteria

* \> 18 years of age on admission to facility
* 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

* Abdominal surgery (within past 30 days prior to switch)
* 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).
Minimum Eligible Age

18 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

No

Sponsors

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Société des Produits Nestlé (SPN)

INDUSTRY

Sponsor Role lead

Responsible Party

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Responsibility Role SPONSOR

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

Site Status

Countries

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Canada

Other Identifiers

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16.06.US.HCN

Identifier Type: -

Identifier Source: org_study_id

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