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Inter-day Reliability of the Oral Glucose Tolerance Test Using Indirect Calorimetry

Inter-day Reliability of the Oral Glucose Tolerance Test Using Indirect Calorimetry

Status
UNKNOWN
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT04320433
Enrollment
20
Registered
2020-03-25
Start date
2020-04-30
Completion date
2020-07-31
Last updated
2020-03-25

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

Conditions

Glucose Intolerance

Brief summary

The main aim of this study is to determine the inter-day reliability, by using indirect calorimetry, of the post-prandial macronutrient oxidation and energy expenditure after consuming oral glucose load solution.

Detailed description

The maintenance of blood glucose concentrations and the oxidation of carbohydrate after consuming carbohydrate is related with a low risk of mortality and morbidity from cardiometabolic diseases. The oral glucose tolerance test is a diagnostic test widely used in the clinical field. However, its inter-day reliability has not been deeply studied. Therefore, it is of clinical interest to study the inter-day reliability of the diagnostic test oral glucose tolerance test using indirect calorimetry and monitoring the response of the glucose levels. 20 young adults will undergo two trials visit with 7 days of separation between conditions. Each evaluation day will conform to the following tests: 1. Basal metabolic rate assessment through indirect calorimetry. 2. Basal heart rate variability through heart rate monitor. 3. Intake of the corresponding glucose load solution. 4. Postprandial nutrient oxidation and energy expenditure assessment through indirect calorimetry 5. Glucose monitoring through Glucose meter.

Interventions

DIAGNOSTIC_TESTOral glucose tolerance test

Participants will ingest 75g anhydrous glucose dissolved in a volume of 200mL of water (NUTER.TEC GLUCOS, Subra, Toulouse, France).

Sponsors

Universidad de Granada
Lead SponsorOTHER

Study design

Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
OTHER
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
18 Years to 30 Years
Healthy volunteers
Yes

Inclusion criteria

* Healthy male or female * Ages 18-30 years * BMI: 18-27.5 kg/m2 * Stable weight over the last 3 months (body weight changes\<35kg) * Participant must be capable and willing to provide consent, understand

Exclusion criteria

, instructions and protocols.

Design outcomes

Primary

MeasureTime frameDescription
Inter-day reliability, 7 days apart, in post-prandial nutrient oxidation7 daysReliability

Secondary

MeasureTime frameDescription
Inter-day reliability, 7 days apart, in post-prandial energy expenditure7 daysReliability
Inter-day reliability, 7 days apart, in glucose levels7 daysReliability

Other

MeasureTime frameDescription
• Reliability of the O2 and CO2 metabolic cart sensors by pure gases infusions using a high-precision mass-flow controllersImmediately after the participants' gas exhange measurementso Inter-day reliability of gas composition (O2 and CO2) measurement by the Omnical® assessed by comparison with a high-precision mass-flow controllers.

Countries

Spain

Contacts

Primary ContactJonatan Ruiz Ruiz, Dr.
ruizj@ugr.es958242754
Backup ContactJuan Manuel Alcantara, PhD student
juanma.alcantara@hotmail.com

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 13, 2026