Trials / Recruiting
RecruitingNCT05829733
6-month Efficacy and Safety of Synolis VA 80/160 in Hip Osteoarthritis
6-month Evaluation of the Efficacy and Safety of Synolis VA 80/160 in the Treatment of Symptomatic Hip Osteoarthritis
- Status
- Recruiting
- Phase
- N/A
- Study type
- Interventional
- Enrollment
- 70 (estimated)
- Sponsor
- Aptissen SA · Industry
- Sex
- All
- Age
- 18 Years
- Healthy volunteers
- Not accepted
Summary
Multicenter, independent study of Synolis VA 80/160 over a period of 6 months
Conditions
Interventions
| Type | Name | Description |
|---|---|---|
| DEVICE | SYNOLIS VA 80/160 | SYNOLIS VA 80/160 (hyaluronic acid 80 mg, sorbitol 160 mg) |
Timeline
- Start date
- 2024-05-27
- Primary completion
- 2027-04-01
- Completion
- 2027-04-01
- First posted
- 2023-04-26
- Last updated
- 2025-12-12
Locations
3 sites across 1 country: France
Source: ClinicalTrials.gov record NCT05829733. Inclusion in this directory is not an endorsement.