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Clinical Trials/NL-OMON22468
NL-OMON22468
Not Yet Recruiting
N/A

An exploratory study investigating the effect of adding an appetite stimulant to an ONS on appetite-related outcomes in older adults residing in nursing homes.

Danone Nutricia Research0 sites45 target enrollmentTBD
ConditionsA

Overview

Phase
N/A
Intervention
Not specified
Conditions
A
Sponsor
Danone Nutricia Research
Enrollment
45
Status
Not Yet Recruiting
Last Updated
last year

Overview

Brief Summary

No summary available.

Registry
who.int
Start Date
TBD
End Date
TBD
Last Updated
last year
Study Type
Interventional

Investigators

Sponsor
Danone Nutricia Research

Eligibility Criteria

Inclusion Criteria

  • 1\.65 years of age or older
  • 2\.Residing in a nursing home
  • 3\.Able to consume high energy and/or high protein ONS at discretion of the Investigator
  • 4\.Written informed consent

Exclusion Criteria

  • 1\.Any known gastrointestinal (GI) disease that interferes with the gastrointestinal motility and nutritional intake, e.g. constipation or diarrhoea secondary to neuropathy, diarrhoea due to chronic inflammatory bowel disease, gastroparesis
  • 2\.Any known metabolic condition that interferes with the breakdown of amino acids
  • 3\.History of GI surgery (except appendectomy) that interferes with the GI function, e.g. ileostomy, colostomy, (partial) gastrectomy or any other procedure for stomach volume reduction, including gastric banding
  • 4\.Investigator’s uncertainty about the willingness or ability of the subject to comply with the protocol requirements, for example due to the presence of a psychiatric disorder (e.g. major depression, psychoses), dementia or Alzheimer’s disease
  • 5\.Known allergy to cow’s milk protein
  • 6\.Known galactosaemia
  • 7\.Known severe lactose intolerance without using lactase
  • 8\.Enrolment in any other studies involving investigational or marketed products concomitantly or within two weeks prior to baseline

Outcomes

Primary Outcomes

Not specified

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