Trials / Completed
CompletedNCT01909037
Exploratory Non Comparative Study to Evaluate the Efficacy of Highly Bioavailable Curcumin (Flexofytol) in Patients With Knee Osteoarthritis
- Status
- Completed
- Phase
- EARLY_Phase 1
- Study type
- Interventional
- Enrollment
- 22 (actual)
- Sponsor
- Tilman S.A. · Industry
- Sex
- All
- Age
- 45 Years – 75 Years
- Healthy volunteers
- Not accepted
Summary
The purpose of this study is to evaluate the efficacy of bio-optimized curcumin(Flexofytol) during a 90-days period in knee ostearthritis patients on the serum levels of specific biomarkers of osteoarthritis and on the evaluation of pain.
Conditions
Interventions
| Type | Name | Description |
|---|---|---|
| DIETARY_SUPPLEMENT | Flexofytol (bio-optimized curcumin) | 2x3 caps/day (before breakfast and in the evening) for 3 months |
Timeline
- Start date
- 2012-03-01
- Primary completion
- 2012-12-01
- Completion
- 2012-12-01
- First posted
- 2013-07-26
- Last updated
- 2015-06-23
Locations
1 site across 1 country: Belgium
Source: ClinicalTrials.gov record NCT01909037. Inclusion in this directory is not an endorsement.