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A Comparison of European and Chinese Blood Sugar Responses

A Comparison of European and Chinese Blood Sugar Responses

Status
UNKNOWN
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT02577874
Enrollment
100
Registered
2015-10-16
Start date
2015-06-30
Completion date
2016-01-31
Last updated
2015-10-16

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Diabetes

Brief summary

This study is designed to compare the responses to an oral glucose challenge between people of European and Chinese heritage (essential participants in the European arm must have tow European parents and likewise for the Chinese participants).

Detailed description

100 participants (50 European and 50 Chinese) will attend a lab after an overnight fast and have a capillary finger-prick blood test to assess fasted blood glucose levels and then consume a 50 gram glucose solution. Blood test will be repeated at 15, 30, 45, 60, 90 and 120 minutes post consumption of the glucose solution. This test will be repeated on a spate occasion at least a week later than the first test. Participants will only take part in the experiment after singing informed consent and agreeing to take part in the study and after a medical screening questionnaire assessing that they are non-diabetic or haemophiliac or have blood born infections.

Interventions

None listed

Sponsors

Sheffield Hallam University
CollaboratorOTHER
Small Changes
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
CROSS_SECTIONAL

Eligibility

Sex/Gender
ALL
Age
19 Years to 59 Years
Healthy volunteers
Yes

Inclusion criteria

* European ethnicity * Chinese ethnicity * age 19-59 years

Exclusion criteria

* diabetics * serious blood born infection * haemophilia

Design outcomes

Primary

MeasureTime frameDescription
Blood sugar response measured by 7 finger prick blood samples2 hours7 finger prick blood samples

Countries

United Kingdom

Contacts

Primary ContactTrevor Simper, DProf
t.simper@shu.ac.uk00 44 2250000
Backup ContactTrevor Simper, DProf
t.simper@shu.ac.uk0044 2250000

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026