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Registry of Avive® Soft Tissue Membrane Utilization in Selected Applications of Acute Trauma of the Upper Extremity

NCT03943134 · Status: TERMINATED · Type: OBSERVATIONAL · Enrollment: 7

Last updated 2025-08-20

No results posted yet for this study

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.

Conditions

  • Acute Upper Extremity Trauma

Interventions

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

Sponsors & Collaborators

  • Axogen Corporation

    lead INDUSTRY

Eligibility

Min Age
5 Years
Max Age
70 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2018-12-01
Primary Completion
2020-12-17
Completion
2020-12-17

Countries

  • United States

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT03943134 on ClinicalTrials.gov