Streamline Occipito-Cervico-Thoracic System Post-Market Clinical Follow-up

Completed

Conditions studied: Spinal Stenosis Occipito-Atlanto-Axial, Spinal Disease, Spinal Stenosis Cervical, Spinal Stenosis Cervicothoracic Region, Spinal Instability

In brief

This is a multi-center, post-market, retrospective study design to collect safety and performance data for patients implanted with the Streamline OCT System.

Key facts

Study ID

NCT04171544

Run by

RTI Surgical

People needed

60

Starts

2019-08-06

Expected to finish

2020-03-31

Last updated by the study team

2020-10-27

Who can join

Age: any. Sex: any. Healthy volunteers: not accepted.

You may qualify if…

• Subject must have had an implant of the OCT System.

You may not qualify if…

• No exclusion criteria.

Where it is running

• Las Vegas Neurosurgical Institute — Las Vegas, Nevada, United States
• Spine Nevada — Reno, Nevada, United States

Full record on ClinicalTrials.gov

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