Trials / Unknown
UnknownNCT02837484
NuTech Affinity™ for the Treatment of Chondral Defects
The NuTech Affinity™ Membrane Product Evaluation for the Treatment of Chondral Defects
- Status
- Unknown
- Phase
- N/A
- Study type
- Interventional
- Enrollment
- 10 (actual)
- Sponsor
- NuTech Medical, Inc · Industry
- Sex
- All
- Age
- 18 Years – 55 Years
- Healthy volunteers
- Not accepted
Summary
This study was designed to evaluate the long term effectiveness of a product used in knee surgery called Affinity™ Membrane.
Detailed description
This is a one-arm prospective, non-randomized, longitudinal study with up to 10 patients from one orthopaedic clinic in the United States. Patients will be treated with Affinity™ a hypothermically preserved amniotic membrane.
Conditions
Interventions
| Type | Name | Description |
|---|---|---|
| OTHER | NuTech Affinity™ Membrane | NuTech Affinity™ Membrane is an aseptically produced hypothermically stored amniotic membrane patch. |
Timeline
- Start date
- 2016-05-01
- Primary completion
- 2020-10-01
- Completion
- 2020-10-01
- First posted
- 2016-07-19
- Last updated
- 2020-01-18
Locations
1 site across 1 country: United States
Source: ClinicalTrials.gov record NCT02837484. Inclusion in this directory is not an endorsement.