MRI Outcomes of VersaWrap Nerve Protector Following Surgery

Part of paid clinical trials in Austin, Texas.

Sponsor
Research Source
Study ID
NCT06942819
Status
Enrolling By Invitation

Conditions

  • Lumbar Decompression

Eligibility Criteria

Sex
ALL
Age
18 Years - 65 Years
Healthy Volunteers
Accepted

Interventions

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

Study Details

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.

Key Dates

Start date
Aug 8, 2025
Status verified
Aug 2025
Primary completion
Dec 1, 2025
Completion
May 1, 2027

Study Design

Enrollment
26 participants (estimated)

Arms

  • Arm: VersaWrap
    All enrolled patients will receive VersaWrap Nerve Protector prior to surgical closure

Primary Outcome Measure

MRI [ Time Frame: 4 months ]

Locations (1)

FacilityCityStateZIPSite coordinators
Austin NeurosurgeonsAustinTexas78746-

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Austin Neurosurgeons· Austin, TX