Retrospective Evaluation of Performance of Coflex® Interlaminer Technology Versus Decompression With or Without Fusion

NCT03041896 · Status: COMPLETED · Type: OBSERVATIONAL · Enrollment: 5050

Last updated 2020-05-19

Study results available
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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.

Conditions

  • Spinal Stenosis

Interventions

DEVICE

coflex® Interlaminar Technology

Interlaminer Technology

Sponsors & Collaborators

  • MCRA

    collaborator INDUSTRY
  • Paradigm Spine

    lead INDUSTRY

Principal Investigators

  • Abigail Allen · MCRA

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2016-07-31
Primary Completion
2017-12-31
Completion
2018-08-31

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT03041896 on ClinicalTrials.gov