At a glance
ClinicalIndex Comparison RecordN/AActive· 932 enrolled
Drug / intervention
Transpedicular Instrumentationprocedure
Likely dose
Not stated in record
Structured eligibility isn't available for this trial yet — see the full criteria in the Eligibility tab below.
Standardized by ClinicalIndex from the ClinicalTrials.gov record · verify against the source.
The European Robotic Spinal Instrumentation (EUROSPIN) Study: A European Prospective Multicenter Multinational Pragmatic Trial on Robot-guided Versus Navigated Versus Freehand Pedicle Screw Fixation
In Brief
An observational study evaluating Transpedicular Instrumentation for Degenerative Disc Disease and 6 related conditions. Active but no longer recruiting, targeting 932 participants across 12 sites in 7 countries.
Detailed Summary
In a multinational prospective study, preoperative, intraoperative, perioperative and follow-up data on patients receiving thoracolumbar pedicle screw placement for degenerative disease or infections or tumors will be collected. The three arms consist of robot-guided (RG), navigated (NV), or freehand (FH) screw insertion.
Study Details
Study Typeobservational
Allocation--
Masking--
Primary Purpose--
ConditionsDegenerative Disc Disease, Spondylolisthesis, Spinal Stenosis, Recurrent Disc Herniation, Spondylodiskitis, Spinal Tumor, Spinal Metastases
CountriesAustria, France, Germany, Italy, Netherlands, Spain, Switzerland
CollaboratorsUniversity Hospital, Zürich
Timeline
N/AActiveOverdue
201820192020202120222023202420252026
First PostedJan 2018
Enrollment StartJan 2019
Primary CompletionJan 2026
Study CompletionMay 2026
TodayJul 2026
First PostedJan 16, 2018
Enrollment StartJan 1, 2019
Primary CompletionJan 30, 2026
Study CompletionMay 1, 2026
TodayJul 2, 2026
Enrollment to primary: 7.1 yearsPosted 8.5 years ago
Interventions
Transpedicular Instrumentationprocedure
Transpedicular screw placement and instrumentation