At a glance
ClinicalIndex Comparison RecordN/ACompleted· 5,050 enrolled
Drug / intervention
coflex® Interlaminar Technologydevice
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.
Retrospective Evaluation of the Clinical and Radiographic Performance of Coflex® Interlaminer Technology Versus Decompression With or Without Fusion.
In Brief
An observational study evaluating coflex® Interlaminar Technology for Spinal Stenosis. Completed, enrolled 5,050 participants.
Detailed Summary
To evaluate clinical, radiologic and patient-reported outcomes who have been treated 1 or 2 levels with the coflex® Interlaminar Technology or decompression with or without fusion.
Study Details
Study Typeobservational
Allocation--
Masking--
Primary Purpose--
ConditionsSpinal Stenosis
Countries--
CollaboratorsMCRA
Timeline
N/ACompletedFinished
2017201820192020202120222023202420252026
Enrollment StartJul 2016
First PostedFeb 2017
Primary CompletionDec 2017
Study CompletionAug 2018
TodayJul 2026
First PostedFeb 3, 2017
Enrollment StartJul 1, 2016
Primary CompletionDec 1, 2017
Study CompletionAug 1, 2018
TodayJul 2, 2026
Enrollment to primary: 1.4 yearsPosted 9.4 years ago
Interventions
coflex® Interlaminar Technologydevice
Interlaminer Technology