CompletedNot Applicable

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

United States60 participantsStarted 2019-08-06

Plain-language summary

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

Who can participate

SexALL

See this in plain English?

AI-rewrites the medical criteria so a patient or caregiver can understand them. Always confirm with the trial site.

Inclusion Criteria: * Subject must have had an implant of the OCT System. Exclusion Criteria: * No exclusion criteria.

What they're measuring

Evaluate time to demonstration of fusion.

Timeframe: 12 months

Trial details

NCT IDNCT04171544

SponsorRTI Surgical

Sponsor typeINDUSTRY

Study typeOBSERVATIONAL

Primary completion2020-03-31

View on ClinicalTrials.gov More Spinal Stenosis Occipito-Atlanto-Axial trials