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The Influence of Sampling Site When Assessing Glucose Tolerance or Insulin Sensitivity With Oral Glucose Ingestion

The Influence of Sampling Site When Assessing Glucose Tolerance or Insulin Sensitivity With Oral Glucose Ingestion

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT02852044
Enrollment
10
Registered
2016-08-02
Start date
2015-11-30
Completion date
2016-09-30
Last updated
2016-10-25

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

Conditions

Hyperglycemia, Insulin Sensitivity

Brief summary

For decades, it has been known that post-meal blood glucose concentrations were associated with the risk of T2D, which was reflected in early diagnostic guidelines. The oral glucose tolerance test (OGTT) has been used since at least 1923 and has remained the most common test for assessing glucose tolerance. Arterial blood (or arterialised blood using heated hand technique) is most appropriate for determining glucose tolerance and insulin sensitivity since this best represents the concentrations of metabolites and hormones that peripheral tissues are exposed to. It is essential to investigate whether venous blood (sometimes used during an OGTT) is representative of arterialised blood during an OGTT, and under different metabolic conditions. The investigators want to understand whether OGTT-derived insulin sensitivity indices differ from venous and arterialised blood; and 2) investigate whether metabolic status (i.e. rest vs lower-limb exercise) influences the difference between forearm venous and arterialised concentrations of glucose and insulin during an OGTT.

Interventions

BEHAVIORALRest

Allowed to watch television or read for one hour prior to oral glucose tolerance test

BEHAVIORALExercise

One hour of cycling at 50% of maximal power output

OTHERDorsal Hand Vein Cannulation (heated hand technique)

Sponsors

University of Bath
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
CROSSOVER
Primary purpose
BASIC_SCIENCE
Masking
NONE

Eligibility

Sex/Gender
MALE
Age
18 Years to 49 Years
Healthy volunteers
Yes

Inclusion criteria

* Aged 18-49 years * Able and willing to safely comply with all study procedures * Able to provide written informed consent for participation

Exclusion criteria

* Diagnosis of any bleeding disorder or taking medication which impacts blood coagulation * The presence of any contraindications to maximal exercise testing, as determined using a physical activity readiness questionnaire (PAR-Q). * Any diagnosis of metabolic disease (i.e. cardiovascular disease or type 2 diabetes).

Design outcomes

Primary

MeasureTime frame
Postprandial plasma glucose concentrations (area under the concentration-time curve)120 mins
OGTT-derived insulin sensitivity120 mins

Secondary

MeasureTime frame
Fasting plasma lactate concentrations5 mins
Fasting plasma triglyceride concentrations5 mins
Postprandial plasma lactate concentrations (area under the concentration-time curve)120 mins
Fasting plasma glucose concentrations5 mins
Substrate utilization for energy provision180 mins
Postprandial plasma insulin concentrations (area under the concentration-time curve)120 mins
Postprandial plasma triglyceride concentrations (area under the concentration-time curve)120 mins
Fasting plasma insulin concentrations5 mins

Countries

United Kingdom

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 26, 2026