Trials / Unknown
UnknownNCT02720159
Early Feasibility Study of the Percutaneous Osseointegrated Prosthesis (POP)
A Prospective, Early Feasibility Study to Characterize the Efficacy and Safety of a Percutaneous Osseointegrated Prosthesis
- Status
- Unknown
- Phase
- N/A
- Study type
- Interventional
- Enrollment
- 10 (estimated)
- Sponsor
- Encore Medical, L.P. · Industry
- Sex
- All
- Age
- 18 Years
- Healthy volunteers
- Not accepted
Summary
The purpose of the clinical study is to characterize the efficacy and safety of a Percutaneous Osseointegrated Prosthesis (POP) device that can provide a satisfactory platform for direct skeletal attachment of prosthetic limbs, which includes a subdermal seal, thus allowing a proper biobarrier around the implant.
Conditions
Interventions
| Type | Name | Description |
|---|---|---|
| DEVICE | Percutaneous Osseintegrated Prosthesis |
Timeline
- Start date
- 2015-12-01
- Primary completion
- 2017-12-01
- First posted
- 2016-03-25
- Last updated
- 2016-03-25
Locations
1 site across 1 country: United States
Source: ClinicalTrials.gov record NCT02720159. Inclusion in this directory is not an endorsement.