Clinical Trials Logo

Clinical Trial Summary

The objective of the study is to compare subjective appetite ratings and after-meal and 24 hour blood glucose levels within overweight and obese female subjects consuming either a standardized 3 day low calorie diet supplemented with a viscous fibre known as PGX (treatment) or a rice flour (placebo control). Each treatment phase will be 3 days in length and separated by 3 week washout phase, so subjects will also be acting as their own control. Subjects will be randomized to either start with the low calorie diet with PGX or the low calorie diet supplemented with rice flour. We hypothesize that the 3 day LCD with PGX will elicit an improved appetite score compared to the 3 day LCD supplemented with the rice flour placebo control.


Clinical Trial Description

n/a


Study Design

Allocation: Randomized, Endpoint Classification: Efficacy Study, Intervention Model: Crossover Assignment, Masking: Double Blind (Subject, Investigator, Outcomes Assessor), Primary Purpose: Treatment


Related Conditions & MeSH terms


NCT number NCT01108328
Study type Interventional
Source Canadian Center for Functional Medicine
Contact
Status Completed
Phase Phase 3
Start date June 2010
Completion date November 2010

See also
  Status Clinical Trial Phase
Completed NCT01580150 - Effects of Berries on Post-meal Blood Sugar N/A
Completed NCT00935350 - Reduction of the Glycemic Index by a Novel Viscous Polysaccharide Phase 2/Phase 3
Completed NCT00801814 - Effect of Escalating Doses of a Novel Viscous Polysaccharide on Postprandial Glycemia Phase 2/Phase 3