Skip to content

Glycaemic Response and Insulinaemic Response for Nutralys S85 Plus and Whey Protein

Glycaemic Response and Insulinaemic Response for Nutralys S85 Plus and Whey Protein

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT04871971
Enrollment
30
Registered
2021-05-04
Start date
2021-09-15
Completion date
2022-08-29
Last updated
2022-09-07

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

Conditions

Healthy

Brief summary

A comparison of the glycaemic response and insulinaemic response to glucose, Nutralys S85 Plus pea protein and whey protein using a single-blind, randomised, repeat measure, crossover design trial.

Detailed description

A single-blind, randomised, repeat measure, crossover design trial will be used to study the glycaemic response and insulinaemic response following consumption of five products: one reference product (50 g available carbohydrate Glucose) and four test products (50 g available carbohydrate Glucose with 10 g NUTRALYS®S85 Plus pea protein, 50 g available carbohydrate Glucose with 20 g NUTRALYS®S85 Plus pea protein, 50 g available carbohydrate Glucose with 10 g Whey protein concentrate and 50 g available carbohydrate Glucose with 20 g Whey protein concentrate).

Interventions

DIETARY_SUPPLEMENT10 g NUTRALYS®S85 Plus pea protein

To determine the glycaemic response and insulinaemic response to 50g Glucose + 10 g NUTRALYS®S85 Plus pea protein.

DIETARY_SUPPLEMENT20 g NUTRALYS®S85 Plus pea protein

To determine the glycaemic response and insulinaemic response to 50g Glucose + 20 g NUTRALYS®S85 Plus pea protein.

DIETARY_SUPPLEMENT10 g Whey protein concentrate

To determine the glycaemic response and insulinaemic response to 50g Glucose + 10 g Whey protein concentrate.

DIETARY_SUPPLEMENT20 g Whey protein concentrate

To determine the glycaemic response and insulinaemic response to 50g Glucose + 20 g Whey protein concentrate.

DIETARY_SUPPLEMENT50 g Glucose

To determine the glycaemic response and insulinaemic response to 50g Glucose

Sponsors

Roquette Freres
CollaboratorINDUSTRY
Oxford Brookes University
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
CROSSOVER
Primary purpose
BASIC_SCIENCE
Masking
SINGLE (Subject)

Masking description

single-blind

Intervention model description

single-blind, randomised, repeat measure, crossover design trial

Eligibility

Sex/Gender
ALL
Age
18 Years to 60 Years
Healthy volunteers
Yes

Inclusion criteria

* Aged 18 to 60 years * Body mass index (BMI) less than 30kg/m2

Exclusion criteria

* Pregnant or lactating * Fasting blood glucose value \> 6.1 mmol/l * Any known food allergy or intolerance * Medical condition(s) or medication(s) known to affect glucose regulation or appetite and/or which influence digestion and absorption of nutrients * Known history of diabetes mellitus or the use of antihyperglycaemic drugs or insulin to treat diabetes and related conditions * Major medical or surgical event requiring hospitalization within the preceding 3 months * Use of steroids, protease inhibitors or antipsychotics (all of which have major effects on glucose metabolism and body fat distribution) * Unable to comply with experimental procedures or did not follow GR testing safety guidelines.

Design outcomes

Primary

MeasureTime frameDescription
Change in blood glucose response from baseline for 3 hours3 hoursChange in postprandial blood glucose response from baseline was measured at 15 min, 30 min, 45 min, 1 hour, 1.5 hours, 2 hours, 2.5 hours and 3 hours
Change in plasma insulin response from baseline for 3 hours3 hoursChange in postprandial plasma insulin response from baseline was measured at 15 min, 30 min, 45 min, 1 hour, 1.5 hours, 2 hours, 2.5 hours and 3 hours
Area under the blood glucose concentration versus time curve3 hoursArea under the blood glucose concentration versus time curve was calculated by trapezoidal rule
Area under the plasma insulin concentration versus time curve3 hoursArea under the plasma insulin concentration versus time curve was calculated by trapezoidal rule
Peak blood glucose concentration (Cmax)0-3 hoursPeak blood glucose concentration (Cmax) after consumption of the test food
Peak plasma insulin concentration (Cmax)0-3 hoursPeak plasma insulin concentration (Cmax) after consumption of the test food
Time of blood glucose peak (Tmax)0-3 hoursTime of blood glucose peak after consumption of the test food
Time of plasma insulin peak (Tmax)0-3 hoursTime of plasma insulin peak after consumption of the test food

Countries

United Kingdom

Outcome results

None listed

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