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Spinal Stenosis Lumbar Coflex PS3

Status: Open to Enrollment
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Study Details

View study details on www.clinicaltrials.gov.

Locations

  • Sacramento

Clinical Trial FAQs

Information for patients and study volunteers, including frequently asked questions.

A 2 and 5 year evaluation of clinical outcomes in the treatment of degenerative spinal stenosis with concomitant low back pain by decompression with additional stabilization using the coflex® Interlaminar Technology for FDA Actual Conditions of Use Study.

A prospective, multi center, concurrently enrolled, propensity score controlled through Month 60. The purpose is to fully characterize safety and efficacy then the coflex device is used in the intended subject population under actual conditions of use.

Rudolph J. Schrot
Rudolph J. Schrot
Principal investigator
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Co-investigator

Sotiris Papamichail

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