Evaluation of an Oral Nutritional Supplement Containing AN777
Status: | Completed |
---|---|
Conditions: | Food Studies, Orthopedic |
Therapuetic Areas: | Pharmacology / Toxicology, Orthopedics / Podiatry |
Healthy: | No |
Age Range: | Any |
Updated: | 2/4/2013 |
Start Date: | February 2011 |
End Date: | July 2012 |
Contact: | Bobbie Swearengin, RN |
Email: | Bobbie.Swearengin@abbott.com |
Phone: | 614 624 7182 |
Evaluation of an Oral Nutritional Supplement Containing AN777 in Malnourished and Frail Subjects
To evaluate the effect of an experimental oral nutritional supplement containing AN777
compared to another oral nutritional supplement in a malnourished, elderly population.
Inclusion Criteria:
- Subject (male or female) is > or equal to 65 and < or equal to 90 years of age
Subject is ambulatory
Subject has a Subjective Global Assessment of B or C
Subject has gait speed <0.8 m/s AND/OR low hand-grip strength
Subject has Class 1 or Class 2 sarcopenia
Subject agrees to refrain from starting a resistance exercise program
Exclusion Criteria:
Subject has type 1 or type 2 diabetes
Subject has inflammatory disease with elevated high sensitivity C-reactive protein
Subject has renal function impairment
Subject reports gastrointestinal disorder (severe chronic diarrhea, nausea, vomiting) that
would preclude ingestion of the study product; an obstruction of the gastrointestinal
tract, inflammatory bowel disease; short bowel syndrome or other major gastrointestinal
disease
Subject reports of current active malignant disease or other significant medical
diagnoses.
Subject reports a history of allergy to any of the ingredients in the study products
Subject reports currently taking medications/dietary supplements/substances that could
profoundly modulate metabolism or weight.
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Creighton University Creighton University, located in Omaha, Neb., offers a top-ranked education in the Jesuit...
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