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MILD® Percutaneous Image-Guided Lumbar Decompression: A Medicare Claims Study

Who can join

Ages 18 and older · All sexes

Inclusion Criteria:

* Medicare beneficiaries receiving MILD or interspinous process decompression
* Diagnosis of LSS with NC

Exclusion Criteria:

* Patients that have received a laminectomy, laminotomy, fusion, interspinous process decompression, or MILD in the lumbar region during the 12 months prior to the index date

About the study

This prospective longitudinal study will compare incidence rates of Medicare beneficiary surgical and minimally invasive intervention post index procedure, as well as harms associated with the MILD procedure, at 24 months post-treatment with MILD, tested against a control group of similar patients that have had a comparable procedure. This study will start with patients treated with a study procedure having an index date on or after January 1, 2017, and enrollment will continue until stopped by the sponsor.

What is being tested

• MILD (device)
• Interspinous Process Decompression (device)

Sponsor: Stryker Instruments · Participants: 8,000 · Started: Mar 10, 2017

Contact the study team

• Angie Lee · Phone: 877-958-6227

Official record on ClinicalTrials.gov — NCT03072927

Locations in the U.S.

Conditions

• Spinal Stenosis

From ClinicalTrials.gov, data retrieved Oct 2, 2026. Each study sets its own eligibility; the study team decides who can join.