CompletedNot Applicable

Effects of Added D-fagomine on Glycaemic Responses to Sucrose

United Kingdom14 participantsStarted 2012-09

Plain-language summary

The purpose of this study is to determine whether D-fagomine affects glycaemic responses to sucrose (commercial white sugar)and quantify the response

Who can participate

Age range18 Years – 55 Years

SexALL

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AI-rewrites the medical criteria so a patient or caregiver can understand them. Always confirm with the trial site.

Inclusion Criteria: * Male or female (not less than 40% Male) * Aged 18 - 55 years * Have a body mass index between 18.5 to 29.99 kg/m2 * Healthy, non-diabetic, no gastric bypass surgery * Have a fasting plasma glucose (finger-stick) \<100 mg/dl (\<5.5 mmol/L) * Willing and able to provide written informed consent Exclusion Criteria: * Smokers * Allergic to dairy or soy

What they're measuring

Postprandial Glycaemic Response Index

Timeframe: 120 minutes

Trial details

NCT IDNCT01811303

SponsorBioglane

Sponsor typeINDUSTRY

Study typeINTERVENTIONAL

Primary completion2013-03

Results submitted2013-04-03

View on ClinicalTrials.gov More Reduction of Post-prandial Glycaemic Response trials