Clinical Outcome Measure at Stryker Spine: COMPASS
Status: Recruiting
Location: See all (7) locations...
Intervention Type: Device
Study Type: Observational
SUMMARY
This is a multicenter, prospective, retrospective, Post Market Clinical Follow-up (PMCF) study in subjects who have undergone or will undergo surgery utilizing one or more Stryker devices according to Stryker cleared Instructions for Use (IFU).
Eligibility
Participation Requirements
Sex: All
Minimum Age: 18
Healthy Volunteers: f
View:
• • To be eligible to participate in the study, the potential subject must meet all inclusion criteria specific to the Stryker system being evaluated, please contact one of the participating investigators or see the device-specific cleared IFU, for further details.
Locations
United States
Florida
Mayo Clinic Florida
RECRUITING
Jacksonville
Maine
MaineHealth Neurosurgery and Spine
RECRUITING
Scarborough
Michigan
Michigan Orthopaedic Surgeons
RECRUITING
Southfield
Ohio
Cleveland Clinc
RECRUITING
Cleveland
Tennessee
Vanderbilt University Medical Center
RECRUITING
Nashville
Texas
Texas Spine & Scoliosis
RECRUITING
Austin
The University of Texas Health Science Center at Houston
RECRUITING
Houston
Contact Information
Primary
Mary Majer
mary.majer@vbspineco.com
866-526-4171
Backup
Effa Gyamfi
effa.gyamfi@vbspineco.com
866-526-4171
Time Frame
Start Date: 2025-01-28
Estimated Completion Date: 2032-01-29
Participants
Target number of participants: 5222
Treatments
S-S-102-A: Cervical Sub-Protocol
The study population includes subjects who are surgically treated with a Stryker device for a cervical condition per the specific device cleared IFUs and Surgical Technique Guides (STGs), by a participating investigator and are willing to complete patient-reported questionnaires at the study-specific time points.
S-S-102-B: Thoracolumbar Sub-Protocol
The study population includes subjects who are surgically treated with a Stryker device for a thoracic/lumbar condition per the specific device cleared IFUs and STGs, by a participating investigator and are willing to complete patient-reported questionnaires at the study-specific time points.
S-S-102-C: Adult Spinal Deformities
The study population includes subjects who are surgically treated with a Stryker device for a spinal deformity condition per the specific device cleared IFUs and STGs, by a participating investigator and are willing to complete patient-reported questionnaires at the study-specific time points.
Related Therapeutic Areas
Sponsors
Leads: VB Spine, LLC