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Strawberry powder (high dose) for Cardiovascular Risk
N/A
Waitlist Available
Research Sponsored by University of Arizona
Eligibility Criteria Checklist
Specific guidelines that determine who can or cannot participate in a clinical trial Must have
Be older than 18 years old
Timeline
Screening 3 weeks
Treatment Varies
Follow Up 4-6 weeks
Awards & highlights
Study Summary
This trial will study the effects of freeze dried strawberry powder on LDL cholesterol, blood pressure, and the gut microbiome in people who are overweight but otherwise healthy.
Timeline
Screening ~ 3 weeks3 visits
Treatment ~ Varies
Follow Up ~ 4-6 weeks
Screening ~ 3 weeks
Treatment ~ Varies
Follow Up ~4-6 weeks
Treatment Details
Study Objectives
Outcome measures can provide a clearer picture of what you can expect from a treatment.Primary outcome measures
Brachial and central blood pressure
LDL-C/non-HDL-C
Secondary outcome measures
Augmentation Index
Glucose
Insulin
+2 moreOther outcome measures
Gut microbiome
Trial Design
3Treatment groups
Experimental Treatment
Active Control
Placebo Group
Group I: Strawberry powder (high dose)Experimental Treatment1 Intervention
40 g/d freeze dried strawberry powder
Group II: Strawberry powder (low dose)Active Control1 Intervention
13 g/d freeze dried strawberry powder
Group III: PlaceboPlacebo Group1 Intervention
40 g/d placebo powder
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Who is running the clinical trial?
University of ArizonaLead Sponsor
514 Previous Clinical Trials
147,970 Total Patients Enrolled
3 Trials studying Cardiovascular Risk
106 Patients Enrolled for Cardiovascular Risk
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