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Completed Phase 3 Interventional

XL TDR® eXtreme Lateral Total Disc Replacement for the Treatment of Lumbar Degenerative Disc Disease (DDD)

ClinicalTrials.gov ID: NCT00927238

Public ClinicalTrials.gov record NCT00927238. Field values are reproduced from the official study page; the official ClinicalTrials.gov record remains the source of truth for eligibility, enrollment, and contact information.

ClinicalTrials.gov public records Last synced Oct 22, 2026, 1:33 PM EDT

Data is sourced from official ClinicalTrials.gov public API records. Always review the official ClinicalTrials.gov record for the latest information.

Official title

A Pivotal, Multi-Center, Clinical Trial Evaluating The Safety And Effectiveness of The Lumbar TDR Device In Patients With Single-Level Lumbar Degenerative Disc Disease

Brief summary

Reproduced verbatim from the official ClinicalTrials.gov record. Not medical advice.

The purpose of this study is to evaluate the safety and effectiveness of XL TDR in patients with single-level degenerative disc disease compared to other devices approved by the FDA for the same or similar indications.

Study identification

NCT ID
NCT00927238
Recruitment status
Completed
Study type
Interventional
Phase
Phase 3
Lead sponsor
NuVasive
Industry
Enrollment
246 participants

Conditions and interventions

Interventions

Device · Other

Eligibility (public fields only)

Age range
18 Years to 70 Years
Sex
All
Healthy volunteers
Healthy volunteers not accepted

This page does not interpret eligibility. Detailed inclusion and exclusion criteria are on the official ClinicalTrials.gov record.

Study timeline

Start date
Jul 2009 (Type not available)
Primary completion
Jul 2014 (Actual)
Completion
Jul 2015 (Actual)
Last update posted
Jul 30, 2015

2009 – 2015

United States locations

U.S. sites
17
U.S. states
14
U.S. cities
17
Facility City State ZIP Site status
Silicon Valley Spine Institute Campbell California 95008 —
Conejo Orthopaedic and Spine Institute Thousand Oaks California 91360 —
Spine Colorado / Durango Orthopedic Associates Durango Colorado 81301 —
Christiana Spine Center Newark Delaware 19713 —
Georgetown University Medical Center Washington D.C. District of Columbia 20007 —
South Florida Spine Institute Miami Beach Florida 33140 —
Southeastern Spine Center & Research Institute Sarasota Florida 34342 —
University of South Florida Tampa Florida 33606 —
West Augusta Spine Specialists Augusta Georgia 30909 —
Spine Institute of Louisiana Shreveport Louisiana 71101 —
Spine Midwest Jefferson City Missouri 65101 —
Western Regional Spine Center for Brain and Spine Surgery Las Vegas Nevada 89109 —
Buffalo Spine Surgery Lockport New York 14094 —
Southern Oregon Orthopedics Medford Oregon 97504 —
Southeastern Spine Institute Mt. Pleasant South Carolina 29464 —
Central Texas Spine Institute Austin Texas 78731 —
Northwest Orthopaedic Specialists Spokane Washington 99208 —

Site contact phone numbers, emails, and investigator names are intentionally not displayed here. Open the official ClinicalTrials.gov record for site contact information.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT00927238, including study identification, conditions, interventions, eligibility (age, sex, healthy volunteer), timeline, and U.S. site list.
What this page does not do
No medical advice, eligibility judgments, treatment recommendations, study quality scoring, or AI-generated medical summaries. No site contact phone numbers, emails, or investigator names.
Where the data comes from
Sourced from the official ClinicalTrials.gov public API. The official record is the source of truth.
Last refresh
Last update posted Jul 30, 2015 · Synced Oct 22, 2026

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Open the official record

The complete public registry record, listed eligibility criteria, and available contact information for NCT00927238 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →