CompletedNot Applicable

Determination of Postprandial Glycemic Responses by Continuous Glucose Monitoring in a Real-World Setting

Germany12 participantsStarted 2018-12-01

Plain-language summary

Self-monitoring of blood glucose using capillary glucose testing has a number of shortcomings compared to continuous glucose monitoring (CGM). We aimed to compare these two methods and used blood glucose measurements in venous blood as a reference. Despite considerable inter-individual variability of postprandial glycemic responses, CGM evaluated postprandial glycemic excursions which had comparable results compared to standard blood glucose measurements under real-life conditions.

Who can participate

Age range18 Years – 80 Years

SexMALE

See this in plain English?

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

Inclusion Criteria: * 18-80 years old Exclusion Criteria: * acute diseases, severe illness with in-patient treatment during the last 3 months, weight change \>2 kg/week during the last month, smoking secession during the last 3 months, drugs for active weight reduction, chronic medication

What they're measuring

Postprandial glucose response

Timeframe: 1 and 2 hours after food consumption

Trial details

NCT IDNCT04147273

SponsorWest German Center of Diabetes and Health

Sponsor typeOTHER

Study typeINTERVENTIONAL

Primary completion2019-05-31

View on ClinicalTrials.gov More Postprandial Glucose Response trials