Expired Study
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W Lafayette, Indiana 47907


Purpose:

This study will be conducted using standardized techniques to collect blood samples via an acute, randomized, cross-over design. Subjects will be provided all of their meals the day prior to testing and participate in 3 testing days with a minimum of 1 week break between testing days and a maximum time commitment of 7 weeks. A trained phlebotomist will place a catheter and collect blood samples from an antecubital vein using sterile techniques.


Criteria:

Inclusion Criteria: 25-39 years old - BMI between 22-37 kg/m2 - Weight stable (± 4.5 kg) for the previous 3 months - Not currently (or within the past 6 months) following a vigorous exercise regimen or weight loss program - No acute illness - Not smoking - Not diabetic - Not pregnant or planning pregnancy in the next 3 months - Lactose tolerant - Willing to limit purposeful activity for 48 hours prior to each testing day - Willing to consume study foods and beverages. Exclusion Criteria: - <25 or >39 years old, BMI <22 or >37 kg/m2 - Currently (or within the past 6 months) following a vigorous exercise regimen greater than -3 - 45 minute exercise sessions per week - Currently following a weight loss program where subject has lost greater than 4.5 kg - Acute illness - Smoking - Diabetic - Pregnant or planning pregnancy in the next 3 months - Lactose intolerant - Unwilling to consume study foods and beverages - Peri and post-menopausal women.


NCT ID:

NCT02506218


Primary Contact:

N/A


Backup Contact:

N/A


Location Contact:

W Lafayette, Indiana 47907
United States



There is no listed contact information for this specific location.

Site Status: N/A


Data Source: ClinicalTrials.gov

Date Processed: November 18, 2017

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