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Stronger Together Global Registry

NCT04364295 · Status: ENROLLING_BY_INVITATION · Type: OBSERVATIONAL · Enrollment: 2285

Last updated 2023-04-04

No results posted yet for this study

Summary

A global, prospective, non-randomized, multicenter, observational, post-market, medical record review registry evaluating real-world evidence for SeaSpine products.

Conditions

  • Spinal Disease

Interventions

DEVICE

Spinal Surgery with SeaSpine product

Implanted with SeaSpine spinal or orthobiologic product

Sponsors & Collaborators

  • SeaSpine, Inc.

    lead INDUSTRY

Principal Investigators

  • Frank Vizesi, PhD · SeaSpine Orthopedics Corporation

Eligibility

Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2020-03-20
Primary Completion
2028-02-29
Completion
2028-08-31
FDA Device
Yes

Countries

  • United States

Study Locations

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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 NCT04364295 on ClinicalTrials.gov