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Fructose and physical inactivity for Vascular Disease
N/A
Waitlist Available
Led By Camila Manrique Acevedo, MD
Research Sponsored by University of Missouri-Columbia
Eligibility Criteria Checklist
Specific guidelines that determine who can or cannot participate in a clinical trial Must have
Be between 18 and 65 years old
Timeline
Screening 3 weeks
Treatment Varies
Follow Up this will be assessed at baseline and at the final visit (10 days)
Awards & highlights
Study Summary
This study is evaluating whether a Westernized lifestyle may have negative impacts for individuals.
Timeline
Screening ~ 3 weeks3 visits
Treatment ~ Varies
Follow Up ~ this will be assessed at baseline and at the final visit (10 days)
Screening ~ 3 weeks
Treatment ~ Varies
Follow Up ~this will be assessed at baseline and at the final visit (10 days)
Treatment Details
Study Objectives
Outcome measures can provide a clearer picture of what you can expect from a treatment.Primary outcome measures
Change in Insulin-stimulated leg blood flow
Secondary outcome measures
Change in Brachial artery flow mediated dilation (FMD)
Change in carotid femoral pulse wave velocity (cfPWV)
Trial Design
1Treatment groups
Experimental Treatment
Group I: Fructose and physical inactivityExperimental Treatment1 Intervention
Subjects will consume 6 cans of soda per day and restrict their physical activity.
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Who is running the clinical trial?
University of Missouri-ColumbiaLead Sponsor
361 Previous Clinical Trials
627,942 Total Patients Enrolled
Camila Manrique Acevedo, MDPrincipal InvestigatorUniversity of Missouri-Columbia
2 Previous Clinical Trials
191 Total Patients Enrolled
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