Cervical Interbody Implant Study

Part of paid clinical trials in Orange, California.

Sponsor
NuVasive
Study ID
NCT04689854
Status
Enrolling By Invitation

Conditions

Eligibility Criteria

Sex
ALL
Age
18 Years - N/A
Healthy Volunteers
Not accepted

Study Details

The primary objective of this study is to evaluate the safety and performance of cervical spine surgery using interbody implants as measured by reported complications, radiographic outcomes, and patient-reported outcomes (PROs).

Key Dates

Start date
Jul 7, 2020
Status verified
Dec 2025
Primary completion
Dec 31, 2025
Completion
Dec 31, 2025

Study Design

Enrollment
150 participants (estimated)

Arms

  • Arm: Cohere Cervical
  • Arm: Modulus Cervical

Primary Outcome Measure

Complications of Interbody Implants [ Time Frame: 24 months ]

Locations (7)

FacilityCityStateZIPSite coordinators
Orthopedic Specialty InstituteOrangeCalifornia92868-
Hartford Healthcare Bone and Joint InstituteHartfordConnecticut06106-
Mass General BrighamSomervilleMassachusetts02145-
Columbia Orthopedic Group ResearchColumbiaMissouri65201-
Duke UniversityDurhamNorth Carolina27710-
Summa HealthAkronOhio44320-
University of VirginiaCharlottesvilleVirginia22908-

Find similar trials in Orange, CA

By research site
Orthopedic Specialty Institute· Orange, CAHartford Healthcare Bone and Joint Institute· Hartford, CTMass General Brigham· Somerville, MAColumbia Orthopedic Group Research· Columbia, MODuke University· Durham, NCSumma Health· Akron, OH

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