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Determination of the postprandial amino acid uptake kinetics of Yoghurt vs Milk: A randomized controlled clinical trial in health individuals - A bioavailability study

Determination of the postprandial amino acid uptake kinetics of Yoghurt vs Milk: A randomized controlled clinical trial in health individuals - A bioavailability study - Nutraferm

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
NL-OMON
Registry ID
NL-OMON57064
Enrollment
16
Registered
2024-10-25
Start date
2024-11-01
Completion date
Unknown
Last updated
2026-02-02

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

Conditions

Gezonde deelnemers, dus geen aandoeningen Not applicable

Interventions

Two study products will be investigated, both commercially available dairy products being a fermented milk product and a non-fermented milk product: Product A: Yoghurt Product B: Full fat pasteuri

Sponsors

Nutricia Research
Lead Sponsor

Eligibility

Age
18 Years to 64 Years

Inclusion criteria

Inclusion criteria: 1. Age >= 18 and = 18.5 and

Exclusion criteria

Exclusion criteria: 1. Any known surgery or ongoing medical condition that interferes significantly with protein absorption and digestion, and/or gastrointestinal (GI) function (e.g. phenylketonuria, pancreatitis, short bowel syndrome, inflammatory bowel disease, gastroesophageal reflux disease, celiac disease, gastric ulcer, chronic gastritis, gastrointestinal cancer, oesophageal and/or gastric surgery), in opinion of the investigator.* 2. Known renal or hepatic diseases that may interfere with protein metabolism, including but not limited to acute hepatitis, chronic liver disease, nephritis, cystinuria, chronic kidney disease, in the opinion of the investigator. 3. Use of systemic medication within the past 3 weeks prior to screening which in the opinion of the investigator may influence gastric acid production and/or gastrointestinal motility or function and/or protein metabolism (for example: antibiotics, anticonvulsants, prokinetics, antacids or gastric acid inhibitors, opioid analgesics, anticoagulants, corticosteroids, laxatives, growth hormone, testosterone, immunosuppressants, or insulin). 4. Known Diabetes Mellitus type I or type II, insulin resistance or metabolic syndrome. 5. Any ongoing cancer and/or cancer treatment*(except for non-melanoma skin cancer or carcinoma in situ).

Design outcomes

Primary

MeasureTime frame
To compare product A vs product B by means of total postprandial blood amino acid concentrations expressed as incremental Area Under the Curve iAUC.

Secondary

MeasureTime frame
o compare product A vs product B by means of essential postprandial blood amino acid (EAA) concentrations expressed as incremental Area Under the Curve iAUC. To compare product A vs product B by means of maximum incremental concentration (iCmax) of total postprandial blood amino acids (TAA) and as time until maximum concentration (Tmax). To compare product A vs product B by means of maximum incremental concentration (iCmax) of essental postprandial blood amino acids (EAA) and as time until maximum concentration (Tmax).

Countries

Netherlands

Outcome results

None listed

Source: NL-OMON (via WHO ICTRP) · Data processed: Feb 7, 2026