Recruiting

Stryker Devices

Sponsor:

VB Spine, LLC

Code:

NCT06226272

Conditions

Degenerative Disc Disease

Degenerative Scoliosis

Eligibility Criteria

Sex: All

Age: 18+

Healthy Volunteers: Not accepted

Interventions

Spinal Fusion

Spinal Fusion

Spinal Deformities Correction

Study Details

Brief 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).

Conditions

Degenerative Disc Disease

Degenerative Scoliosis

Study ID

NCT06226272

Start date

Jan 28, 2025

Status verified date

Jun, 2026

Completion date

Jan 29, 2032

Anticipated

Primary completion date

Jan 29, 2029

Anticipated

Eligibility Criteria

Eligibility Criteria

Sex: All

Age: 18+

Healthy Volunteers: Not accepted

Inclusion Criteria:

• 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.

Exclusion Criteria:

• The exclusion criteria are based on the contraindications as presented in the Stryker device cleared IFUs, please contact one of the participating investigators or see the device-specific cleared IFU, for further details.

Study Design

Enrollment

5222 participants

Anticipated

Interventions and Outcome Measures

Arms

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.

Interventions

Spinal Fusion

Cervical Spinal Fusion

Spinal Fusion

Thoracic / Lumbar Spinal Fusion

Spinal Deformities Correction

Spinal Deformities Correction

Primary outcome measure

  • S-S-102-A [ Time Frame: Baseline through 24-months post-op. ]
  • S-S-102-B [ Time Frame: Baseline through 24-months post-op. ]
  • S-S-102-C [ Time Frame: Baseline through 24-months post-op. ]

Central Contacts and Locations

Central contacts

Mary Majer

866-526-4171mary.majer@vbspineco.com

Effa Gyamfi

866-526-4171effa.gyamfi@vbspineco.com

Locations

Mayo Clinic Florida

Recruiting

Jacksonville, Florida, United States, 32224

Contacts

Megan Gauthier

gauthier.megan2@mayo.edu

Principal Investigator:

Stephen Pirris, MD

MaineHealth Neurosurgery and Spine

Recruiting

Scarborough, Maine, United States, 04074

Contacts

Chelsea Ruel

chelsea.ruel@mainehealth.org

Principal Investigator:

Robert D. Ecker, MD

Michigan Orthopaedic Surgeons

Recruiting

Southfield, Michigan, United States, 48033

Contacts

Reily Nesson

reily@researchtex.com

Principal Investigator:

Jad Khalil, MD

Cleveland Clinc

Recruiting

Cleveland, Ohio, United States, 44195

Contacts

Research Coordinator

216-445-1741robinsn8@ccf.org

Principal Investigator:

Ghaith Habboub, MD

Vanderbilt University Medical Center

Recruiting

Nashville, Tennessee, United States, 37232

Contacts

Richard Call

richard.call@vumc.org

Principal Investigator:

Amir M Abtahi, MD

Texas Spine & Scoliosis

Recruiting

Austin, Texas, United States, 78705

Contacts

Devender Singh, PhD

dpsingh@ascension.org

Principal Investigator:

Eeric Truumees, MD

The University of Texas Health Science Center at Houston

Recruiting

Houston, Texas, United States, 77030

Contacts

Keyla Guevara

Keyla.D.Guevara@uth.tmc.edu

Minal Bhadane, PhD

(419) 377-4566minal.bhadane.1@uth.tmc.edu

Principal Investigator:

James E. Showery, MD

More Information

Sponsor

VB Spine, LLC

Last update posted

Jun 26, 2026

Last verified

Jun, 2026

Keywords

  • Device: Cervical or Thoracolumbar Spinal fusion
  • Device: Adult Spinal Deformities

Trial information was received from ClinicalTrials.gov and was last updated on 2026-10-06. This information was provided to ClinicalTrials.gov by VB Spine, LLC on 2026-06-26. Recruitment status is synced daily from ClinicalTrials.gov and may not reflect the sponsor's current status. Confirm during your call.