Clinical Trials Directory

Trials / Completed

CompletedNCT06232460

An Open Label, Dose-escalation Study, Assessing the Safety and Tolerability of a Collagen Peptide

Status
Completed
Phase
N/A
Study type
Interventional
Enrollment
60 (actual)
Sponsor
Rousselot BVBA · Industry
Sex
All
Age
18 Years – 60 Years
Healthy volunteers
Accepted

Summary

This study evaluates the safety and tolerability of three different doses (5 g, 10 g and 20 g) of a collagen powder in healthy adults over a 12-week period.

Detailed description

This study evaluates the safety and tolerability of three different doses (5 g, 10 g and 20 g) of a collagen powder, each for 4-weeks in healthy adults over a 12-week period by measuring occurrence of adverse events, safety blood panel, vital signs, occurrence of common gastrointestinal symptom's and the Gastrointestinal Symptom Rating Scale

Conditions

Interventions

TypeNameDescription
DIETARY_SUPPLEMENTH805g, 10g \& 20g

Timeline

Start date
2024-02-08
Primary completion
2024-07-29
Completion
2024-07-29
First posted
2024-01-30
Last updated
2025-05-09

Locations

1 site across 1 country: United States

Source: ClinicalTrials.gov record NCT06232460. Inclusion in this directory is not an endorsement.