MRI Outcomes of VersaWrap Nerve Protector Following Surgery

NCT06942819 · Status: ENROLLING_BY_INVITATION · Type: OBSERVATIONAL · Enrollment: 26

Last updated 2025-08-22

No results posted yet for this study

Summary

The purpose of this study is to evaluate enhancement patterns in magnetic resonance imaging (MRI) evidence following the use of VersaWrap in bilateral lumbar decompression surgeries.

Conditions

  • Lumbar Decompression

Interventions

DEVICE

VersaWrap Nerve Protector

VersaWrap Nerve Protector is applied to the nerve root to protect the surrounding tissues

Sponsors & Collaborators

  • Research Source

    lead NETWORK

Eligibility

Min Age
18 Years
Max Age
65 Years
Sex
ALL
Healthy Volunteers
Yes

Timeline & Regulatory

Start
2025-08-08
Primary Completion
2025-12-01
Completion
2027-05-01
FDA Device
Yes

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 NCT06942819 on ClinicalTrials.gov