Treatment of One and/or Two Level Cervical Degenerative Disc Disease

Part of paid clinical trials in Fort Worth, Texas.

Sponsor
Research Source
Study ID
NCT05812092
Status
Enrolling By Invitation

Conditions

  • Cervical Radiculopathy

Eligibility Criteria

Sex
ALL
Age
18 Years - N/A
Healthy Volunteers
Accepted

Interventions

  • CONDUIT Interbody Cervical System with DePuy Synthes Cervical Plating System — DEVICE
    CONDUIT Interbody Cervical System will be inserted between C2 through T1 and fixated using a DePuy Synthes Cervical Plating System at 1 or 2 levels.

Study Details

The objective of this study is to collect clinical and radiographic outcomes using the CONDUIT™ Interbody Cervical System with supplemental fixation using a DePuy Synthes Cervical Plating System.

Key Dates

Start date
May 1, 2021
Status verified
Aug 2025
Primary completion
Mar 1, 2027
Completion
Mar 1, 2027

Study Design

Enrollment
50 participants (estimated)

Arms

  • Arm: DePuy Synthes Cervical Plating System
    All enrolled patients will receive CONDUIT Interbody Cervical System with supplemental fixation using a DePuy Synthes Cervical Plating System.

Primary Outcome Measure

Primary Outcome Measure: [ Time Frame: 12 months ]

Locations (1)

FacilityCityStateZIPSite coordinators
DFW Center for Spinal DisordersFort WorthTexas76132-

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DFW Center for Spinal Disorders· Fort Worth, TX

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