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Prebiotic
Prebiotic oligofructose-enriched inulin for Obesity
N/A
Waitlist Available
Led By Raylene A Reimer, PhD, RD
Research Sponsored by University of Calgary
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 baseline and 6 months
Awards & highlights
Study Summary
This trial will test whether prebiotics can improve knee function and reduce pain in obese adults with metabolic knee osteoarthritis.
Eligible Conditions
- Obesity
- Osteoarthritis
Timeline
Screening ~ 3 weeks3 visits
Treatment ~ Varies
Follow Up ~ baseline and 6 months
Screening ~ 3 weeks
Treatment ~ Varies
Follow Up ~baseline and 6 months
Treatment Details
Study Objectives
Outcome measures can provide a clearer picture of what you can expect from a treatment.Primary outcome measures
Change in 30 second chair stand test
Change in 40 metre fast based walk
Change in 6 minute walk test
+2 moreSecondary outcome measures
Change in body fat
Change in fecal microbiota composition
Change in fecal short chain fatty acids (SCFA) concentration
+8 moreOther outcome measures
Change in gastrointestinal comfort
Trial Design
2Treatment groups
Experimental Treatment
Placebo Group
Group I: PrebioticExperimental Treatment1 Intervention
Two 8g doses/day (12 kcal/dose) of oligofructose-enriched inulin
Group II: PlaceboPlacebo Group1 Intervention
Two 3.3g doses/day (12 kcal/dose) of maltodextrin
Treatment
First Studied
Drug Approval Stage
How many patients have taken this drug
Prebiotic oligofructose-enriched inulin
2018
N/A
~60
Find a Location
Who is running the clinical trial?
University of CalgaryLead Sponsor
792 Previous Clinical Trials
869,100 Total Patients Enrolled
14 Trials studying Obesity
1,102 Patients Enrolled for Obesity
Raylene A Reimer, PhD, RDPrincipal InvestigatorUniversity of Calgary
6 Previous Clinical Trials
413 Total Patients Enrolled
2 Trials studying Obesity
174 Patients Enrolled for Obesity
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