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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 change between the beginning and the end of each treatment (12 weeks each)
Awards & highlights
Study Summary
This trial will test the hypothesis that 4 weeks of oral intake of CC can modulate the gut microbiota and protect against obesity and associated metabolic disorders in humans.
Eligible Conditions
- Obesity
- Non-alcoholic Fatty Liver Disease
- Metabolic Syndrome
- Insulin Resistance
- Microtia
- Endotoxemia
Timeline
Screening ~ 3 weeks3 visits
Treatment ~ Varies
Follow Up ~ change between the beginning and the end of each treatment (12 weeks each)
Screening ~ 3 weeks
Treatment ~ Varies
Follow Up ~change between the beginning and the end of each treatment (12 weeks each)
Treatment Details
Study Objectives
Outcome measures can provide a clearer picture of what you can expect from a treatment.Primary outcome measures
Change in Gut Microbiota Composition and Diversity
Change in fat accumulation in the liver
Secondary outcome measures
Change in Endotoxemia
Change in Glucose homeostasis
Change in Inflammation state of the tissue
+13 moreTrial Design
2Treatment groups
Experimental Treatment
Placebo Group
Group I: Camu camuExperimental Treatment1 Intervention
Group II: PlaceboPlacebo Group1 Intervention
Treatment
First Studied
Drug Approval Stage
How many patients have taken this drug
Camu camu
2020
N/A
~40
Find a Location
Who is running the clinical trial?
Laval UniversityLead Sponsor
417 Previous Clinical Trials
172,237 Total Patients Enrolled
33 Trials studying Obesity
16,292 Patients Enrolled for Obesity
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