Clinical Trials Directory

Trials / Completed

CompletedNCT06971484

Glucosamine Sulfate Bioavailability

Comparative Bioavailability of Crystalline and Regular Glucosamine Sulfate: A Randomized Crossover Study in Healthy Adults

Status
Completed
Phase
N/A
Study type
Interventional
Enrollment
10 (actual)
Sponsor
Isura · Academic / Other
Sex
All
Age
21 Years – 65 Years
Healthy volunteers
Accepted

Summary

This study aims to compare the pharmacokinetics and bioavailability of crystalline glucosamine sulfate and regular glucosamine sulfate using a double-blind, randomized, crossover design.

Conditions

Interventions

TypeNameDescription
DIETARY_SUPPLEMENTCrystalline glucosamine sulfateA maximum single dose of 1500mg of glucosamine sulfate in a caplet.
DIETARY_SUPPLEMENTRegular glucosamine sulfateA maximum single dose of 1500mg of glucosamine sulfate in hard gel capsules.

Timeline

Start date
2025-01-06
Primary completion
2025-03-28
Completion
2025-04-30
First posted
2025-05-14
Last updated
2025-05-22

Locations

1 site across 1 country: Canada

Source: ClinicalTrials.gov record NCT06971484. Inclusion in this directory is not an endorsement.