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ACTIVE NOT RECRUITING
NCT06876311

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

Sponsor: Silony Medical GmbH

View on ClinicalTrials.gov

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.

Official title: Sponsor-initiated, Retrospective, Monocentric, Non-interventional Clinical Observational Study to Evaluate the STALIF® C FLX, STALIF® M FLX, STALIF® L FLX Cages and FORTOS-C®

Key Details

Gender

All

Age Range

21 Years - Any

Study Type

OBSERVATIONAL

Enrollment

100

Start Date

2025-03-04

Completion Date

2025-05-30

Last Updated

2025-03-14

Healthy Volunteers

No

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

Locations (1)

Golden State Orthopedics and Spine

San Ramon, California, United States