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ACTIVE NOT RECRUITING

Registry of Avance® Nerve Graft's Utilization and Recovery Outcomes Post Peripheral Nerve Reconstruction

NCT01526681 · View on ClinicalTrials.gov ↗

Study Summary

This study is a registry of general use of Avance Nerve Graft and is intended to evaluate the uses, response rates, and safety of Avance Nerve Graft in the real-life clinical setting. Optional addendums 1 and 2 included in the protocol are intended to establish comparative groups and focused subgroups within the registry.

Conditions Studied

Interventions

  • OTHER Processed Human Nerve Graft
  • OTHER Standard Treatment, Autogenous Nerve Graft, Direct Suture, etc.
  • OTHER Autogenous Nerve Graft
  • DEVICE Nerve Tube Conduit
  • PROCEDURE Autologous Breast Reconstruction with Neurotization

Study Locations (20)

California

  • RANGER & MATCH: University of California - Irvine — Orange
  • RANGER & MATCH: The Buncke Clinic — San Francisco
  • Sensation-NOW: Stanford University — Stanford

Maryland

  • RANGER: Johns Hopkins University — Baltimore
  • Sensation-NOW: Johns Hopkins University — Baltimore
  • RANGER: Walter Reed National Military Medical Center — Bethesda

Arizona

  • RANGER & MATCH: Arizona Center for Hand Surgery — Phoenix
  • RANGER: Phoenix Children's Hospital — Phoenix

Florida

  • RANGER: University of Miami — Miami
  • RANGER & MATCH: Florida Orthopaedic Institute — Tampa

Kansas

  • RANGER & MATCH: University of Kansas Medical Center — Kansas City
  • Sensation-NOW: University of Kansas Medical Center — Kansas City

Colorado

  • Sensation-NOW: University of Colorado School of Medicine — Aurora

District of Columbia

  • Sensation-NOW: George Washington University — Washington D.C.

Georgia

  • RANGER: Hand & Upper Extremity Center of Georgia/Children's Hospital of Atlanta — Atlanta

Trial Details

FieldValue
Enrollment Target 3,126 participants
Start Date 2008-11
Est. Completion 2028-11

Sponsor

Axogen Corporation

4 total trials

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Full Details on ClinicalTrials.gov ↗

What the Registry Record Tells You About NCT01526681

The ClinicalTrials.gov registry entry for NCT01526681 describes a study currently listed as active not recruiting. It is categorized as an unspecified phase, which is the standard way researchers label where a study sits along the investigational pathway from early safety work through later efficacy and post-marketing evaluation. The registered enrollment target is 3,126 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is Axogen Corporation, which has 4 total studies on file at ClinicalTrials.gov, and sponsors are the parties responsible for study design, oversight, and regulatory filings.

The record links to 1 condition, with Peripheral Nerve Injuries appearing as the primary indexed condition, and to 5 interventions — of which Processed Human Nerve Graft is the first listed. Interventions can include drugs, devices, procedures, behavioral programs, or observational arms, and each is tracked as a separate registry field so that downstream queries can filter accurately. When a trial lists multiple interventions, it usually reflects a multi-arm design or a comparison protocol rather than a single treatment being tested in isolation. The brief summary published in the registry is the clearest source of protocol intent and should be read before drawing conclusions from any sidebar tags.

Geographic footprint matters for practical reasons: NCT01526681 reports 20 study locations spanning 13 distinct geographic areas — top geographies include California, Maryland, Arizona. A larger site network tends to correlate with broader recruitment capacity, but it does not imply anything about study quality, and site-level enrollment status can diverge from the overall registry status shown above. Every data point on this page comes from the public ClinicalTrials.gov dataset and is reproduced here for reference only; it is not a medical recommendation, an endorsement of the sponsor, or an invitation to enroll. Verify current status, eligibility criteria, and contact details directly at ClinicalTrials.gov, and discuss any participation decision with your own healthcare provider.

Frequently Asked Questions

What is clinical trial NCT01526681 about?

NCT01526681 is a clinical study titled "Registry of Avance® Nerve Graft's Utilization and Recovery Outcomes Post Peripheral Nerve Reconstruction". This study is a registry of general use of Avance Nerve Graft and is intended to evaluate the uses, response rates, and safety of Avance Nerve Graft in the real-life clinical setting. Optional addendums 1 and 2 included in the protocol are intended to establish comparative groups and focused subgrou...

What is the current status of trial NCT01526681?

This trial is currently active not recruiting. The enrollment target is 3,126 participants. The study started on 2008-11. Estimated completion is 2028-11.

What conditions does trial NCT01526681 study?

This clinical trial studies the following conditions: Peripheral Nerve Injuries. These conditions were identified from the trial registry and reflect the primary focus areas of the research.

What interventions are being tested in trial NCT01526681?

The interventions under investigation include: Processed Human Nerve Graft (OTHER), Standard Treatment, Autogenous Nerve Graft, Direct Suture, etc. (OTHER), Autogenous Nerve Graft (OTHER), Nerve Tube Conduit (DEVICE), Autologous Breast Reconstruction with Neurotization (PROCEDURE). Each intervention is being evaluated for safety and efficacy as part of this clinical study.

Who is sponsoring clinical trial NCT01526681?

This trial is sponsored by Axogen Corporation, which has 4 total clinical trials registered on ClinicalTrials.gov. The sponsor is responsible for the study's design, funding, and regulatory compliance.

Where is trial NCT01526681 being conducted?

This trial has 20 study locations across Arizona, California, Colorado, District of Columbia, Florida. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.

Related

Data sourced from official U.S. government datasets. See our methodology for details. Retrieved and formatted by PlainTrial Editorial