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Artificial Disc Replacement

PRESTIGE LP™ Cervical Disc for Cervical Disc Degeneration

N/A

Waitlist Available

Research Sponsored by Medtronic Spinal and Biologics

Eligibility Criteria Checklist

Specific guidelines that determine who can or cannot participate in a clinical trial

Must have

Be older than 18 years old

Timeline

Screening 3 weeks

Treatment Varies

Follow Up 3, 6, and 12 months

Awards & highlights

Study Summary

This trial will study how much metal is in the blood of people who got surgery with a certain kind of medical device. The data will be used to improve safety for people using this device in the future.

Eligible Conditions

Cervical Disc Degeneration
Myelopathy
Radiculopathy

Timeline

Screening ~ 3 weeks3 visits

Treatment ~ Varies

Follow Up ~ 3, 6, and 12 months

Screening ~ 3 weeks

Treatment ~ Varies

Follow Up ~3, 6, and 12 months

This trial's timeline: 3 weeks for screening, Varies for treatment, and 3, 6, and 12 months for reporting.

Treatment Details

Study Objectives

Outcome measures can provide a clearer picture of what you can expect from a treatment.

Primary outcome measures

Concentrations of Titanium, Vanadium, and Aluminum in the Blood Serum

Secondary outcome measures

Neck Pain and Arm Pain

Number of Participants Who Achieved NDI Success

Number of Participants Who Achieved Neurological Success

+2 more

Trial Design

1Treatment groups

Experimental Treatment

Group I: PRESTIGE LPExperimental Treatment1 Intervention

Patients receive surgical treatment with the PRESTIGE LP™ Cervical Disc at two contiguous cervical levels from C3-C7.

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Find a Location

Who is running the clinical trial?

Medtronic Spinal and BiologicsLead Sponsor

55 Previous Clinical Trials

10,563 Total Patients Enrolled

Frequently Asked Questions

These questions and answers are submitted by anonymous patients, and have not been verified by our internal team.

How many participants are being taken on for this experimental program?

"Medtronic Spinal and Biologics is sponsoring this clinical trial, in order to obtain data from 30 participants who meet their inclusion criteria. The study sites are located at Kellogg M.D., Brain & Spine (Portland, Oregon) as well as Todd H. Lanman, M.D., INC.(Beverly Hills, California)."

Answered by AI

Are there any opportunities for patients to participate in this experiment at present?

"Affirmative, the information on clinicaltrials.gov suggests that this experiment is presently recruiting patients. The study was initially published on June 6th 2018 and has been refreshed as of July 29th 2022 with a goal to recruit 30 participants from 3 distinctive locations."

Answered by AI

Recent research and studies

clinicaltrials.govStudy

An Investigation of the Metal Concentration in Patients Implanted With the PRESTIGE LP™ Cervical Disc at Two Contiguous Levels in the Cervical Spine

2018. "An Investigation of the Metal Concentration in Patients Implanted With the PRESTIGE LP™ Cervical Disc at Two Contiguous Levels in the Cervical Spine". ClinicalTrials.gov. https://clinicaltrials.gov/ct2/show/NCT03062657.