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OpenTrials
Completed

NCT Number: NCT03459001

Evaluation of a High Calorie, High Protein Tube Feeding Product in an Adult Population With or at Risk of Malnutrition

This prospective, observational study is designed to observe the use of a high calorie, high protein tube feed product in adults that are malnourished or at risk of malnutrition, as assessed by a clinician, and have been placed on a nutritional care plan which includes a tube feeding formula, per standard of care.

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Key information

Age range

18 year and older

Sex eligibility

All sexes

Study type

Observational

Primary location

Residencia Albertia Moratalaz, Madrid, Spain

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Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Malnourished or at risk for malnutrition based on the Malnutrition Universal Tool (MUST) score ≥ 2.
  • Under the care of a health care professional for malnutrition or at risk of malnutrition and has been prescribed the study formula.
  • Requires and agrees to be tube fed the enteral feeding product for at least 16 consecutive days as their sole-source of nutritional intake.
  • Free living in the community or is residing in a nursing home.
  • Conforms to the requirements set forth on the study product label.

Exclusion criteria

  • Currently taking or has taken antibiotics within 2 weeks prior to enrollment.
  • Consuming food PO.
  • Current active cancer and the study physician determines that the subject is not suitable for the study.
  • History of diabetes mellitus as evidenced by taking anti-hyperglycemic medications or by self-reported dietary modification for control of diabetes mellitus.
  • Renal or liver failure.
  • Pregnant as demonstrated by self-report.
  • Severe auto immune disease (per physician's discretion) and is on immuno-modulating therapy.
  • History of allergy to any of the ingredients in the study product.
  • Active Human Immunodeficiency Virus (HIV).
  • Known dementia, brain metastases, eating disorders, history of significant neurological or psychiatric disorder, or any other psychological condition that may interfere with study product consumption and does not have a caregiver who can assist them with adherence to the study protocol.
  • Condition that is contraindicated to tube feeding the study product.
  • Taking part in a non-approved clinical trial.

Treatment and study plan

Tube Feeding Product

Other

a high calorie, high protein tube feed product consumed sole source per their physician's recommendation and per standard of care

Primary outcomes

  1. Tube Feed Product Compliance

    Time frame: Day 1 to Day 20

    Average Daily Intake and Proportion of Days Compliant

Secondary outcomes

  1. Adverse Events

    Time frame: Day 0 to Day 20

    Non serious AE and SAE collection

  2. Body Mass Index

    Time frame: Day 0 to Day 20

    Weight, Height

Sponsors and collaborators

Lead sponsor

Abbott Nutrition

Industry

Registry information

Official study title

A Prospective, Observational Study to Evaluate the Use of a High Calorie, High Protein Tube Feeding Product in an Adult Population With or at Risk of Malnutrition

Important dates

Study start
2018
Primary completion
2019
Study completion
2019
First posted
Mar 8, 2018
Registry last updated
Apr 19, 2019

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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