Status:

COMPLETED

Spine Patient Outcomes Registry for Biomet/EBI (Electro-Biology, Inc)

Lead Sponsor:

Zimmer Biomet

Conditions:

Degenerative Disc Disease

Spinal Stenosis

Eligibility:

All Genders

Brief Summary

The purpose of this patient registry is to prospectively collect data on patients who are having spinal surgery with EBI and Interpore Cross Spine Products.

Detailed Description

A patient registry to prospectively collect data on patients who are having spinal surgery with EBI and Interpore Cross Spine Products.

Eligibility Criteria

Inclusion

  • N/A

Exclusion

  • N/A

Key Trial Info

Start Date :

April 1 2004

Trial Type :

OBSERVATIONAL

Allocation :

ACTUAL

End Date :

December 6 2007

Estimated Enrollment :

651 Patients enrolled

Trial Details

Trial ID

NCT00726284

Start Date

April 1 2004

End Date

December 6 2007

Last Update

February 24 2020

Active Locations (5)

Enter a location and click search to find clinical trials sorted by distance.

Page 1 of 2 (5 locations)

1

Neurological Surgery Associates

Little Rock, Arkansas, United States, 72205

2

Florida Orthopedics Association

Orange City, Florida, United States, 32763

3

CNS Healthcare

Akron, Ohio, United States, 44333

4

Oklahoma Spine and Brain

Tulsa, Oklahoma, United States, 74132

Spine Patient Outcomes Registry for Biomet/EBI (Electro-Biology, Inc) | DecenTrialz