Trials / Terminated
TerminatedNCT03943134
Registry of Avive® Soft Tissue Membrane Utilization in Selected Applications of Acute Trauma of the Upper Extremity
A Multicenter, Ambispective, Clinical Outcomes Registry Study of Avive® Soft Tissue Membrane Utilization in Selected Applications of Acute Trauma of the Upper Extremity
- Status
- Terminated
- Phase
- —
- Study type
- Observational
- Enrollment
- 7 (actual)
- Sponsor
- Axogen Corporation · Industry
- Sex
- All
- Age
- 5 Years – 70 Years
- Healthy volunteers
- Not accepted
Summary
A registry study to evaluate the role of Avive® Soft Tissue Membrane in the management of nerve injury associated with acute trauma in the upper extremity.
Detailed description
This is a multicenter outcomes registry study of Avive® Soft Tissue Membrane in the management of nerve injuries associated with selected upper extremity acute trauma. The study will evaluate clinical condition, economic impact, and functional outcomes.
Conditions
Interventions
| Type | Name | Description |
|---|---|---|
| OTHER | Minimally Processed Human Umbilical Cord Membrane | Implantation of minimally processed human umbilical cord membrane at the time of surgery |
| OTHER | Standard Surgical Procedures | Standard surgical intervention for at least one targeted acute upper extremity trauma |
Timeline
- Start date
- 2018-12-01
- Primary completion
- 2020-12-17
- Completion
- 2020-12-17
- First posted
- 2019-05-09
- Last updated
- 2025-08-20
Locations
3 sites across 1 country: United States
Source: ClinicalTrials.gov record NCT03943134. Inclusion in this directory is not an endorsement.