Lumbar & Sacroiliac Fusion Study Involving Previously Implanted Devices

Part of paid clinical trials in Overland Park, Kansas.

Sponsor
Spinal Simplicity LLC
Study ID
NCT07204288
Status
Recruiting
Apply to this trial

Conditions

  • Fusion of Spine
  • Sacroiliac; Fusion

Eligibility Criteria

Sex
ALL
Age
18 Years - N/A
Healthy Volunteers
Not accepted

Interventions

  • Cat Scan, if applicable — OTHER
    CT imaging is being used to assess fusion in participants with previously implanted devices that were not explanted.

Study Details

This study is a multi-center, observational, prospective and retrospective data collection study

Key Dates

Start date
Sep 11, 2025
Status verified
Mar 2026
Primary completion
Aug 31, 2026
Completion
Dec 31, 2026

Study Design

Enrollment
500 participants (estimated)
Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
OTHER

Arms

  • Other: Previously implanted with lumbar and/or sacroiliac fusion device(s)
    This study will involve patients previously commercially implanted with Minuteman G5 MIS fusion plate, the Liberty sacroiliac fusion device, and/or the Patriot sacroiliac fusion device. Subjects will undergo a CT scan, if applicable and PROs.

Primary Outcome Measure

Investigate radiographic outcomes [ Time Frame: Enrollment ]

Central Contacts

Locations (3)

FacilityCityStateZIPSite coordinators
Crimson Pain ManagementOverland ParkKansas66209
Morteza Rabii, NP
Daniel Kloster, MD (PRINCIPAL_INVESTIGATOR)
Nuroscience Research CenterOverland ParkKansas66210
Amy Reinert
Mayank Gupta, MD (PRINCIPAL_INVESTIGATOR)
Nura Precision Pain ManagementEdinaMinnesota55435
Ken Farmer
R. Scott Stayner, MD (PRINCIPAL_INVESTIGATOR)

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Crimson Pain Management· Overland Park, KSNuroscience Research Center· Overland Park, KSNura Precision Pain Management· Edina, MN

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