UnknownNot Applicable

The Fixation Study

United States50 participantsStarted 2020-03-05

Plain-language summary

To perform a clinical evaluation of safety and performance for the SeaSpine Non- Cervical Pedicle Screw Systems

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: * Have undergone surgery * Have undergone at least 12-months of postoperative follow-up Exclusion Criteria: * Any condition that the Investigator determines is unacceptable

What they're measuring

The primary outcome for the study is device performance.

Timeframe: 12 months post-operative

Trial details

NCT IDNCT04300777

SponsorSeaSpine, Inc.

Sponsor typeINDUSTRY

Study typeOBSERVATIONAL

Primary completion2021-06-30

View on ClinicalTrials.gov More Degenerative Conditions, Neurologic trials