NuVasive® ACP System Study

Study Purpose

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

Recruitment Criteria

Accepts Healthy Volunteers Healthy volunteers are participants who do not have a disease or condition, or related conditions or symptoms	Unknown
Study Type An interventional clinical study is where participants are assigned to receive one or more interventions (or no intervention) so that researchers can evaluate the effects of the interventions on biomedical or health-related outcomes. An observational clinical study is where participants identified as belonging to study groups are assessed for biomedical or health outcomes. Searching Both is inclusive of interventional and observational studies.	Observational
Eligible Ages	18 Years and Over
Gender	All

More Inclusion & Exclusion Criteria

Inclusion Criteria:

1. Patients who are ≥18 years of age at the time of consent. 2. Have planned anterior cervical (C2 to C7) spine surgery using the NuVasive ACP System in conjunction with a NuVasive interbody implant or vertebral body replacement device (VBR), or a structural bone allograft spacer, for treatment of any of the following conditions: 1. degenerative disc disease, as defined by neck pain of discogenic origin with degeneration of the disc confirmed by patient history and radiographic studies. 2. trauma (including fractures) 3. tumors involving the cervical spine. 4. cervical spinal deformity (kyphosis, lordosis, or scoliosis) 5. failed previous cervical fusion(s) (e.g., pseudoarthrosis) 6. cervical spondylolisthesis. 7. cervical spinal stenosis. 3. Able to undergo surgery based on physical exam, medical history, and surgeon judgment. 4. Understands the conditions of enrollment and is willing to sign an informed consent form to participate in the study.

Exclusion Criteria:

1. Procedures performed with interbody implants with integrated vertebral body screw(s) 2. Patient is involved in active litigation relating to the spine (worker's compensation claim is allowed if it is not contested) 3. Use of bone growth stimulators postoperatively. 4. Active smoking within 6 weeks of surgery. 5. Patient has known sensitivity to materials implanted. 6. Systemic or local infection (latent or active) or signs of local inflammation. 7. Patient has inadequate bone stock or quality, or a physical or medical condition that would prohibit beneficial surgical outcome based on surgeon judgment. 8. Pregnant, or plans to become pregnant. 9. Patient is a prisoner. 10. Patient is participating in another clinical study that would confound study data

Trial Details

Trial ID: This trial id was obtained from ClinicalTrials.gov, a service of the U.S. National Institutes of Health, providing information on publicly and privately supported clinical studies of human participants with locations in all 50 States and in 196 countries.	NCT05066711
Phase Phase 1: Studies that emphasize safety and how the drug is metabolized and excreted in humans. Phase 2: Studies that gather preliminary data on effectiveness (whether the drug works in people who have a certain disease or condition) and additional safety data. Phase 3: Studies that gather more information about safety and effectiveness by studying different populations and different dosages and by using the drug in combination with other drugs. Phase 4: Studies occurring after FDA has approved a drug for marketing, efficacy, or optimal use.
Lead Sponsor The sponsor is the organization or person who oversees the clinical study and is responsible for analyzing the study data.	NuVasive
Principal Investigator The person who is responsible for the scientific and technical direction of the entire clinical study.	Kyle Malone, MS
Principal Investigator Affiliation	NuVasive
Agency Class Category of organization(s) involved as sponsor (and collaborator) supporting the trial.	Industry
Overall Status	Enrolling by invitation
Countries	United States
Conditions The disease, disorder, syndrome, illness, or injury that is being studied.	Cervical Spondylosis, Cervical Radiculopathy, Cervical Myelopathy, Cervical Disc Disease, Cervical Stenosis, Cervical Disc Herniation, Cervical Spine Disease

Additional Details

This study is a prospective, uncontrolled, multicenter study to evaluate the safety and performance of the NuVasive ACP System in patients who undergo anterior cervical spine surgery. Consecutive patients at a given site who meet eligibility requirements will be asked to consent to participate in the study. These patients will present with pathologic conditions in the cervical spine that are amenable to surgical treatment and will be screened prior to study enrollment. Once enrolled in the study, subjects will undergo anterior cervical spine surgery using the NuVasive ACP System based on the surgeon's standard of care. At least 75 subjects will be enrolled and will be followed for 24 months after the surgery.

Arms & Interventions

Arms

: ACP System

Interventions

Contact a Trial Team

If you are interested in learning more about this trial, find the trial site nearest to your location and contact the site coordinator via email or phone. We also strongly recommend that you consult with your healthcare provider about the trials that may interest you and refer to our terms of service below.

Duly Health and Care, Naperville, Illinois

Status

Address

Duly Health and Care

Naperville, Illinois, 60540

Columbia Orthopedic Group Research, Columbia, Missouri

Status

Address

Columbia Orthopedic Group Research

Columbia, Missouri, 65201

Atlantic Brain and Spine, Wilmington, North Carolina

Status

Address

Atlantic Brain and Spine

Wilmington, North Carolina, 28401

Clinical Trial Finder