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
| Type | Name | Description |
|---|---|---|
| DIETARY_SUPPLEMENT | Crystalline glucosamine sulfate | A maximum single dose of 1500mg of glucosamine sulfate in a caplet. |
| DIETARY_SUPPLEMENT | Regular glucosamine sulfate | A 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.