MedTrace Logo

Observational Study to Evaluate the STALIF® C FLX, STALIF® M FLX, STALIF® L FLX Cages and FORTOS-C®

NCT06876311 · Status: ACTIVE_NOT_RECRUITING · Type: OBSERVATIONAL · Enrollment: 100

Last updated 2025-03-14

No results posted yet for this study

Summary

Post-operative clinical outcome data on the devices used to treat spinal diseases are collected and evaluated in order to analyze the safety and performance of the implants used.

Conditions

  • Degenerative Cervical Disc Disease
  • Degenerative Lumbar Diseases

Interventions

DEVICE

Anterior Cervical Interbody Fusion

Standard Anterior Cervical Interbody Fusion with Stand-alone Cervical Cages

DEVICE

Anterior lumbar Interbody Fusion

Standard Anterior Lumbar Interbody Fusion with Stand-Alone Lumbar Cages

DEVICE

Lateral Lumbar Interbody Fusion

Standard Lateral Lumbar Interbody Fusion with Stand-alone Lumbar cage

Sponsors & Collaborators

  • Silony Medical GmbH

    lead INDUSTRY

Eligibility

Min Age
21 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2025-03-04
Primary Completion
2025-04-30
Completion
2025-05-30
FDA Device
Yes

Countries

  • United States

Study Locations

More Related Trials

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 NCT06876311 on ClinicalTrials.gov