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To evaluate the sensations experienced by subjects consuming a nutritional beverage.
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| Label | Type | Description | Intervention Names |
|---|---|---|---|
| Nutritional Beverage #2 | Experimental | Nutritional Beverage with an amino acid Oral 237 ml |
|
| Nutritional Beverage #3 | Experimental | Nutritional Beverage with an amino acid Oral 237 ml |
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| Nutritional Beverage #1 | Placebo Comparator | Nutritional Beverage Oral 237 ml |
|
| Name | Type | Description | Arm Group Labels | Other Names |
|---|---|---|---|---|
| Nutritional Beverage | Other | Nutritional Beverage Oral 237mL |
| |
| Measure | Description | Time Frame |
|---|---|---|
| Proportion of subjects experiencing neurologic adverse event(s) | 2-3 weeks |
| Measure | Description | Time Frame |
|---|---|---|
| Proportion of subjects experiencing any adverse event(s). | 2-3 Weeks |
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Inclusion Criteria:
Subject ≥ 45 years of age.
If female, subject is either postmenopausal for at least 1 year or surgically sterile
Subject reports that he/she has not participated in a research study in the last three months.
Exclusion Criteria:
Subject has active metabolic or endocrine disease
Subject has an autoimmune disorder
Subject has a disorder of gastrointestinal tract or any gastrointestinal surgery in past 12 months.
Subject has food allergy, celiac disease or intolerance to any of the ingredients in the study products
Subject reports history of parasthesia; and/or is currently taking medication/dietary supplements/substances that may cause parasthesia for 4 weeks prior to screening
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| Name | Affiliation | Role |
|---|---|---|
| Vikkie Mustad, PhD | Abbott | Study Chair |
| Facility | Status | City | State | ZIP | Country | Contacts |
|---|---|---|---|---|---|---|
| The National Food Lab | Livermore | California | 94551 | United States |
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| Nutritional Beverage |
| Other |
Nutritional Beverage Oral 237 mL |
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| Nutritional Beverage | Other | Nutritional Beverage Oral 237mL |
|