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NCT00642876 · ClinicalTrials.gov registry record · NA

PRESTIGE® Cervical Disc Study

A NA study, sponsored by Medtronic Spinal and Biologics.

Completed
Registry status
NA
Development phase
541
Enrollment target

NCT00642876: Completed NA study, sponsored by Medtronic Spinal and Biologics.

NCT00642876 is a NA study that has completed, run by Medtronic Spinal and Biologics. The registered enrollment target is 541 participants, below the 1,404-participant average among 58,714 other NA trials with a reported enrollment target (61% lower). According to ClinicalTrials.gov, the official US trial registry.

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The verdict

NCT00642876, a NA study, has completed, sponsored by Medtronic Spinal and Biologics.

COMPLETED
Registry status
NA
Development phase
541 participants
Enrollment target

Study Summary

The purpose of this clinical investigation is to evaluate the safety and effectiveness of the ACD in the single level surgical treatment of patients with symptomatic cervical degenerative disc disease. The primary follow-up information obtained from this clinical investigation are used to support a PMA application for the ACD.

Interventions

  • DEVICE Allograft Fusion and ATLANTIS™ Cervical Plate System
  • DEVICE PRESTIGE® Cervical Disc

Trial Details

FieldValue
Enrollment Target 541 participants
Start Date 2002-10
Est. Completion 2013-05
Phase NA
Medtronic Spinal and Biologics

26 total trials

What the finished NCT00642876 record still lists

NCT00642876 is an interventional study that assigns participants to a tested intervention. The registered 541 participants enrollment target is mid-sized for trials with a published cap, below the 1,404-participant average among 58,714 other NA trials with a reported enrollment target (61% lower).

The record links to 0 conditions, and to 2 interventions - of which Allograft Fusion and ATLANTIS™ Cervical Plate System is the first listed.

NCT00642876 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT00642876 about?

NCT00642876 is a clinical study titled "PRESTIGE® Cervical Disc Study". The purpose of this clinical investigation is to evaluate the safety and effectiveness of the ACD in the single level surgical treatment of patients with symptomatic cervical degenerative disc disease. The primary follow-up information obtained from this clinical investigation are used to support a ...

What is the current status of trial NCT00642876?

This trial is currently completed. It is a NA study. The enrollment target is 541 participants. The study started on 2002-10. Estimated completion is 2013-05.

What interventions are being tested in trial NCT00642876?

The interventions under investigation include: Allograft Fusion and ATLANTIS™ Cervical Plate System (DEVICE), PRESTIGE® Cervical Disc (DEVICE).

Who is sponsoring clinical trial NCT00642876?

This trial is sponsored by Medtronic Spinal and Biologics, which has 26 total clinical trials registered on ClinicalTrials.gov.

How this trial's enrollment target compares

Where NCT00642876's enrollment target sits among peer trials

541 187th of 2000 higher than 1,814 of 2,000 other NA trials

participants (enrollment target), bucketed by value

Each bar is a band; taller bars hold more other NA trials. The dashed line + filled bar mark this entry. Hover or tap any bar for its full count and share, and where it sits relative to this entry.

Source ClinicalTrials.gov registry export · 2026-08-08

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Source: ClinicalTrials.gov NCT00642876, the US trial registry maintained by the National Library of Medicine. NCT00642876 (mid enrollment · none site footprint · completed) retrieved and formatted by PlainTrial, see methodology.