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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.
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Inclusion criteria
25-39 years old
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Interventional model
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12 participants in 3 patient groups
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Data sourced from clinicaltrials.gov
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