Status:

COMPLETED

Impact of the Source and Food Matrices on the Bioavailability of Peptan® (Collagen Peptides) in Healthy Subjects

Lead Sponsor:

Rousselot BVBA

Collaborating Sponsors:

BioTeSys GmbH

Conditions:

Bioavailability

Eligibility:

All Genders

18-50 years

Phase:

NA

Brief Summary

The aim of this study is the comparison of the oral bioavailability of hydroxyproline, a key marker for collagen peptide intake, after ingestion of collagen peptides from different sources, sizes and ...

Detailed Description

The absorption (blood) of collagen peptides from bovine, fish and porcine source in different sizes and administered together with foods of different polyphenol content will be assessed. Pharmacokinet...

Eligibility Criteria

Inclusion

  • Main
  • Subject is able and willing to sign the Informed Consent Form prior to screening evaluations
  • Sex: female and male (50 % of each gender)
  • Age: 18-50 years
  • BMI ≥19 and ≤28 kg/m²
  • Nonsmoker
  • Main

Exclusion

  • Relevant history or presence of any severe medical disorder, potentially interfering with this study (e.g. mal absorption, chronic gastro-intestinal diseases, heavy depression, diabetes, acute cancers within last 3 years except basal cell carcinoma of the skin, etc.)
  • Significant changes in lifestyle or medication (within last 3 mo.) or surgical intervention or surgical procedure such as bariatric surgery
  • Application of corticoids (intravenously, orally or intraarticularly) and other immune-suppressing drug (within last 2 weeks)
  • Blood donation within 1 month prior to study start or during study
  • Regular intake of drugs or supplements possibly interfering with this study (Glucosamine, chondroitin sulfate, hyaluronic acid, omega-3, folic acid, curcumin/turmeric, Boswellia serrata, collagen, Vitamin D) within 2 weeks prior to study start or during study
  • Intake of anticoagulants like Heparin, Marcumar etc.
  • Coffee consumption \>3 cups / day
  • History of hypersensitivity to fish

Key Trial Info

Start Date :

September 20 2019

Trial Type :

INTERVENTIONAL

Allocation :

ACTUAL

End Date :

October 25 2019

Estimated Enrollment :

6 Patients enrolled

Trial Details

Trial ID

NCT04097808

Start Date

September 20 2019

End Date

October 25 2019

Last Update

April 30 2020

Active Locations (1)

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BioTeSys GmbH

Esslingen am Neckar, Germany, 73728