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RECRUITING

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

NCT03072927 · View on ClinicalTrials.gov ↗

Study Summary

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.

Conditions Studied

Interventions

  • DEVICE MILD
  • DEVICE Interspinous Process Decompression

Study Locations (20)

Alabama

  • Athens-Limestone Hospital — Athens
  • North Baldwin Infirmary — Bay Minette
  • Southside Pain Specialists — Birmingham
  • St Vincents Birmingham — Birmingham
  • The Univ of Alabama At Birmingham — Birmingham
  • Birmingham Surgery Center — Birmingham
  • Alabama Ortho Spine and Sports — Birmingham
  • Outpatient Services East — Birmingham
  • St Vincents One Nineteen Health and — Birmingham
  • Decatur Ambulatory Surgery Center — Decatur
  • Baldwin County Surg Ctr — Fairhope
  • Gardendale Surgical Center — Gardendale
  • Highland Medical Center — Scottsboro
  • Tuscaloosa Surgery Center — Tuscaloosa

Arizona

  • Bullhead City Community Hosp — Bullhead City
  • Arizona Specialty Surgery Center — Chandler
  • Chandler Surgical Ctr PLC — Chandler
  • Advanced Pain Modalities — Chandler

Alaska

  • AA Spine & Pain Clinic — Anchorage
  • Copper Basin Surg Ctr — Wasilla

Trial Details

FieldValue
Enrollment Target 8,000 participants
Start Date 2017-03-10
Est. Completion 2026-12

Sponsor

Stryker Instruments

2 total trials

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Full Details on ClinicalTrials.gov ↗

What the Registry Record Tells You About NCT03072927

The ClinicalTrials.gov registry entry for NCT03072927 describes a study currently listed as recruiting. It is categorized as an unspecified phase, which is the standard way researchers label where a study sits along the investigational pathway from early safety work through later efficacy and post-marketing evaluation. The registered enrollment target is 8,000 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is Stryker Instruments, which has 2 total studies on file at ClinicalTrials.gov, and sponsors are the parties responsible for study design, oversight, and regulatory filings.

The record links to 1 condition, with Lumbar Spinal Stenosis appearing as the primary indexed condition, and to 2 interventions — of which MILD is the first listed. Interventions can include drugs, devices, procedures, behavioral programs, or observational arms, and each is tracked as a separate registry field so that downstream queries can filter accurately. When a trial lists multiple interventions, it usually reflects a multi-arm design or a comparison protocol rather than a single treatment being tested in isolation. The brief summary published in the registry is the clearest source of protocol intent and should be read before drawing conclusions from any sidebar tags.

Geographic footprint matters for practical reasons: NCT03072927 reports 20 study locations spanning 3 distinct geographic areas — top geographies include Alabama, Arizona, Alaska. A larger site network tends to correlate with broader recruitment capacity, but it does not imply anything about study quality, and site-level enrollment status can diverge from the overall registry status shown above. Every data point on this page comes from the public ClinicalTrials.gov dataset and is reproduced here for reference only; it is not a medical recommendation, an endorsement of the sponsor, or an invitation to enroll. Verify current status, eligibility criteria, and contact details directly at ClinicalTrials.gov, and discuss any participation decision with your own healthcare provider.

Frequently Asked Questions

What is clinical trial NCT03072927 about?

NCT03072927 is a clinical study titled "MILD® Percutaneous Image-Guided Lumbar Decompression: A Medicare Claims 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 t...

What is the current status of trial NCT03072927?

This trial is currently recruiting. The enrollment target is 8,000 participants. The study started on 2017-03-10. Estimated completion is 2026-12.

What conditions does trial NCT03072927 study?

This clinical trial studies the following conditions: Lumbar Spinal Stenosis. These conditions were identified from the trial registry and reflect the primary focus areas of the research.

What interventions are being tested in trial NCT03072927?

The interventions under investigation include: MILD (DEVICE), Interspinous Process Decompression (DEVICE). Each intervention is being evaluated for safety and efficacy as part of this clinical study.

Who is sponsoring clinical trial NCT03072927?

This trial is sponsored by Stryker Instruments, which has 2 total clinical trials registered on ClinicalTrials.gov. The sponsor is responsible for the study's design, funding, and regulatory compliance.

Where is trial NCT03072927 being conducted?

This trial has 20 study locations across Alabama, Alaska, Arizona. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.

Related

Data sourced from official U.S. government datasets. See our methodology for details. Retrieved and formatted by PlainTrial Editorial