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Clinical Outcome Measure at Stryker Spine

NCT06226272 · Status: NOT_YET_RECRUITING · Type: OBSERVATIONAL · Enrollment: 5222

Last updated 2024-04-16

No results posted yet for this study

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

Interventions

DEVICE

Spinal Fusion

Cervical Spinal Fusion

DEVICE

Spinal Fusion

Thoracic / Lumbar Spinal Fusion

DEVICE

Spinal Deformities Correction

Spinal Deformities Correction

Sponsors & Collaborators

  • Stryker Spine

    lead INDUSTRY

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2024-05-06
Primary Completion
2029-01-29
Completion
2032-01-29
FDA Device
Yes

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT06226272 on ClinicalTrials.gov