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COMPLETED NA

Activ-L™ Artificial Disc Treatment of Degenerative Disc Disease in the Treatment of Degenerative Disc Disease

NCT00589797 · View on ClinicalTrials.gov ↗

Study Summary

The purpose of this study is to learn whether an investigational device called the Activ-L Artificial Disc is safe and effective in the treatment of degenerative disc disease of the lower (lumbar) spine.

Conditions Studied

Interventions

  • DEVICE Activ-L Artificial Disc
  • DEVICE ProDisc-L Total Disc Replacement or Charité Artificial Disc

Study Locations (17)

California

  • Scripps Memorial Hospital La Jolla — La Jolla
  • Hoag Memorial Hospital Presbyterian — Newport Beach
  • Rancho Specialty Hospital — Rancho Cucamonga
  • University of California San Francisco — San Francisco
  • St. John's Hospital and Health Center — Santa Monica

Florida

  • Aventura Hospital and Medical Center — Aventura
  • University Community Hospital — Tampa

Illinois

  • Rush University Medical Center — Chicago
  • Neurosciences Education and Research Foundation — Peoria

Colorado

  • University of Colorado Health Sciences Center — Aurora

Connecticut

  • Yale University School of Medicine/New Haven Hospital — New Haven

Minnesota

  • HealthEast St. John's Hospital — Maplewood

New York

  • Hospital for Special Surgery — New York

North Carolina

  • Carolinas Healthcare — Charlotte

Trial Details

FieldValue
Enrollment Target 376 participants
Start Date 2007-01
Est. Completion 2017-01
Phase NA

Sponsor

Aesculap Implant Systems

1 total trials

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Full Details on ClinicalTrials.gov ↗

What the Registry Record Tells You About NCT00589797

The ClinicalTrials.gov registry entry for NCT00589797 describes a study currently listed as completed. It is categorized as NA, which is the standard way researchers label where a study sits along the investigational pathway from early safety work through later efficacy and post-marketing evaluation. The registered enrollment target is 376 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is Aesculap Implant Systems, which has 1 total studies on file at ClinicalTrials.gov, and sponsors are the parties responsible for study design, oversight, and regulatory filings.

The record links to 1 condition, with Degenerative Disc Disease appearing as the primary indexed condition, and to 2 interventions — of which Activ-L Artificial Disc is the first listed. Interventions can include drugs, devices, procedures, behavioral programs, or observational arms, and each is tracked as a separate registry field so that downstream queries can filter accurately. When a trial lists multiple interventions, it usually reflects a multi-arm design or a comparison protocol rather than a single treatment being tested in isolation. The brief summary published in the registry is the clearest source of protocol intent and should be read before drawing conclusions from any sidebar tags.

Geographic footprint matters for practical reasons: NCT00589797 reports 17 study locations spanning 11 distinct geographic areas — top geographies include California, Florida, Illinois. A larger site network tends to correlate with broader recruitment capacity, but it does not imply anything about study quality, and site-level enrollment status can diverge from the overall registry status shown above. Every data point on this page comes from the public ClinicalTrials.gov dataset and is reproduced here for reference only; it is not a medical recommendation, an endorsement of the sponsor, or an invitation to enroll. Verify current status, eligibility criteria, and contact details directly at ClinicalTrials.gov, and discuss any participation decision with your own healthcare provider.

Frequently Asked Questions

What is clinical trial NCT00589797 about?

NCT00589797 is a clinical study titled "Activ-L™ Artificial Disc Treatment of Degenerative Disc Disease in the Treatment of Degenerative Disc Disease". The purpose of this study is to learn whether an investigational device called the Activ-L Artificial Disc is safe and effective in the treatment of degenerative disc disease of the lower (lumbar) spine.

What is the current status of trial NCT00589797?

This trial is currently completed. It is a NA study. The enrollment target is 376 participants. The study started on 2007-01. Estimated completion is 2017-01.

What conditions does trial NCT00589797 study?

This clinical trial studies the following conditions: Degenerative Disc Disease. These conditions were identified from the trial registry and reflect the primary focus areas of the research.

What interventions are being tested in trial NCT00589797?

The interventions under investigation include: Activ-L Artificial Disc (DEVICE), ProDisc-L Total Disc Replacement or Charité Artificial Disc (DEVICE). Each intervention is being evaluated for safety and efficacy as part of this clinical study.

Who is sponsoring clinical trial NCT00589797?

This trial is sponsored by Aesculap Implant Systems, which has 1 total clinical trials registered on ClinicalTrials.gov. The sponsor is responsible for the study's design, funding, and regulatory compliance.

Where is trial NCT00589797 being conducted?

This trial has 17 study locations across California, Colorado, Connecticut, Florida, Illinois. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.

Related

Data sourced from official U.S. government datasets. See our methodology for details. Retrieved and formatted by PlainTrial Editorial