CompletedInterventionalNot ApplicableUpdated Mar 5, 2021
Evaluation of AN777 in Elderly Subjects | NCT00798291 | Trialant
CompletedInterventionalPhase 2Phase 3Updated Mar 22, 2010
Evaluation of AN777 in Elderly Subjects
Evaluation of AN777 in Elderly Subjects
ClinicalTrials.gov ID
NCT00798291
Lead Sponsor
Abbott NutritionINDUSTRY
Overall Status
Completed
Study Type
Interventional
Phase
Phase 2Phase 3
Enrollment
108Estimated
Last Update Posted
Mar 22, 2010Estimated
Start Date
Oct 2008
Primary Completion Date
Dec 2009Actual
Completion Date
Jan 2010Actual
Official Title
Evaluation of AN777 in Elderly Subjects
Brief Summary
To evaluate whether AN777 with or without exercise affects muscle mass change in elderly subjects.
Aged
Ad lib diet and Control placebo
Ad lib diet and An 777
Ad lib diet/ placebo/ exercise
Ad lib diet; AN 777; exercise
Ages Eligible for Study
Older Adult (65+)
Sexes Eligible for Study
All
Accepts Healthy Volunteers
Yes
Eligibility Criteria
Inclusion Criteria:
Subject (male or female) is at least 65 years of age
Subject has a Geriatric Nutritional Risk Index (GNRI)of 92 or over
Subject has Body Mass Index (BMI) > 20.0 but <30.0
Subject is ambulatory
Subject agrees to maintain current activity level
Exclusion Criteria:
Subject has undergone major surgery, less than 4 weeks prior to enrollment in the study
Subject has current active malignant disease, except basal or squamous cell skin carcinoma or carcinoma in situ of the uterine cervix
Subject has stated immunodeficiency disorder
Subject has stated history of diabetes
Subject has stated presence of partial or full artificial limb
Subject has stated kidney disease
Subject has stated history of uncontrollable hypertension
Subject had myocardial infarction within the last 3 months
Subject had recent antibiotic use (within 1 week prior to screening).
Subject has a history of allergy to any of the ingredients in the study products
Subject has an obstruction of the gastrointestinal tract precluding ingestion of the study product, inflammatory bowel disease, short bowel syndrome or other major gastrointestinal disease
Subject has stated uncontrolled severe diarrhea, nausea or vomiting
Subject has untreated clinically significant ascites, pleural effusion or edema
Subject has 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
Subject is actively pursuing weight loss
Subject is currently taking medications/dietary supplements/substances that could profoundly modulate metabolism or weight Exceptions for multi-vitamin/mineral supplement, inhaled steroids for asthma or chronic obstructive pulmonary disease, topical or optical steroids and short-term use (less than two weeks) of dexamethasone
Primary Purpose
Treatment
Allocation
Randomized
Interventional Model
Factorial Assignment
Masking
Quadruple
No central contacts
There are no central contacts for this study.
Department of Health and Exercise Science, University of Oklahoma