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The Coflex®COMMUNITY Study: An Observational Study of Coflex® Interlaminar Technology

NCT02457468 · Status: COMPLETED · Type: OBSERVATIONAL · Enrollment: 325

Last updated 2019-12-24

No results posted yet for this study

Summary

The purpose of the coflexCOMMUNITY observational study is to collect information on patients with spinal stenosis undergoing back surgery with the coflex® implant, and to look at their outcomes and the cost-effectiveness of this procedure.

Conditions

  • Spinal Stenosis

Interventions

DEVICE

coflex

Sponsors & Collaborators

  • SPIRITT Research

    collaborator UNKNOWN

  • Predicted, Reported and Observed Outcomes Foundation

    lead OTHER

Eligibility

Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2015-06-30
Primary Completion
2019-12-31
Completion
2019-12-31

Countries

  • United States

Study Locations

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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 NCT02457468 on ClinicalTrials.gov