CI

At a glance

ClinicalIndex Comparison Record
N/ACompleted· 139 enrolled
Drug / intervention
lumbar spinal arthroplasty + Maverick™procedure
Likely dose
Not stated in record
Structured eligibility isn't available for this trial yet — see the full criteria in the Eligibility tab below.

Standardized by ClinicalIndex from the ClinicalTrials.gov record · verify against the source.

Search/NCT01338493
NCT01338493N/ACompleted
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Maverick Total Disc Replacement in a 'Real World' Patient Population - A Prospective, Multicenter, Observational Study

Medtronic Spinal and Biologics·observational·Posted Apr 19, 2011·Updated Jan 28, 2016

In Brief

An observational study evaluating lumbar spinal arthroplasty + Maverick™ for Degenerative Disc Disease. Completed, enrolled 139 participants across 13 sites in 3 countries.

Detailed Summary

The primary purpose of the study is to document the reduction of disability after Maverick total disc replacement surgery in a 'real-world' patient population requiring disc replacement.

Study Details

Study Typeobservational
Allocation--
Masking--
Primary Purpose--
ConditionsDegenerative Disc Disease
CountriesCanada, France, Germany
Collaborators--

Timeline

N/ACompletedFinished
200920102011201220132014201520162017201820192020202120222023202420252026
First PostedApr 19, 2011
Enrollment StartFeb 1, 2009
Primary CompletionJul 1, 2013
TodayJul 2, 2026
Enrollment to primary: 4.4 yearsPosted 15.2 years ago

Interventions

lumbar spinal arthroplasty + Maverick™procedure

All patients will be subjected to a lumbar spinal arthroplasty. The anterior lumbar spine is approached through either a transperitoneal or retroperitoneal exposure. A complete anterior discectomy is performed and the Maverick™ Artificial Disc System is inserted to replace the damaged lumbar intervertebral disc.