Trials / Completed
CompletedNCT01535144
Comparative Study of Osteosynthesis for Chevron Osteotomy of Hallux Valgus Using Degradable Versus Non-degradable Metallic Device
- Status
- Completed
- Phase
- N/A
- Study type
- Interventional
- Enrollment
- 26 (actual)
- Sponsor
- Syntellix AG · Industry
- Sex
- All
- Age
- 40 Years – 79 Years
- Healthy volunteers
- Not accepted
Summary
The purpose of the study is to show the equivalence of a new degradable metallic device to a non-degradable metallic device in patients with Hallux Valgus.
Conditions
Interventions
| Type | Name | Description |
|---|---|---|
| DEVICE | Fracture compressing screw ZfW 102 Königsee Implantate GmbH | Comparison of two metallic implantable fracture compressing screws |
| DEVICE | Fracture compressing screw titanium Königsee Implantate GmbH | Comparison of two metallic implantable fracture compressing screws |
Timeline
- Start date
- 2010-02-01
- Primary completion
- 2012-02-01
- Completion
- 2012-02-01
- First posted
- 2012-02-17
- Last updated
- 2012-03-01
Locations
1 site across 1 country: Germany
Source: ClinicalTrials.gov record NCT01535144. Inclusion in this directory is not an endorsement.