Trial Details

Not Recruiting
Basic Information
Clinical ID c4971
Identifier ISRCTN82579275
Trial Title Occipitocervical spine stabilization using PERLA posterior occipito-cervico-thoracic fixation. A post-market clinical follow-up study
Trial URL Visit Original Page
Study Information
Study Results

Yes

Conditions Acute or chronic cranio-cervical junction instability due to, but not limited to: Trauma: Atlanto-occipital dislocation, occipital condyle fracture, atlas, and axis fractures; Inflammation/autoimmune disease: Rheumatoid arthritis, psoriatic arthritis, ank
Interventions Any patient who has received a Perla Occipital system in the participating center will be asked for the data collection of their retrospective data.
Participant Information
Sponsor Spineart (Switzerland)
City NULL
Country/Region Austria;France;Germany
Enrollment Criteria
Sex Requirement ALL
Age Requirement NULL
Study Design
Study Type Observational
Phase PHASE4
Time Information
Start Date NULL
Primary Completion Date NULL
Completion Date NULL