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The European Robotic Spinal Instrumentation (EUROSPIN) Study

Study acronym: EUROSPIN
StatusActive, Not Recruiting
PhaseNot specified
Started
View on ClinicalTrials.gov ↗

Record History

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  1. Notable Results first posted: Mar 31, 2026v8 Show 9 more changesShow less
    • Primary completion date changed from estimate of Sep 1, 2021 to Jan 30, 2026
    • Start date: Feb 20, 2018 to Jan 1, 2019
    • Trial status: Recruiting to Active, Not Recruiting
    • Enrollment target: estimated 615 to confirmed 932
    • Study sites: 13 to 12
    • Study completion date: Sep 1, 2023 to May 1, 2026
    • Secondary endpoints revised (12)
    • Primary endpoint revised
    • Collaborators expanded, about 3 words
  2. Notable Primary completion date: Jan 1, 2021 to Sep 1, 2021
    • Study completion date: Jan 1, 2023 to Sep 1, 2023
    v7
  3. Minor Site contacts updated at 1 of 13 sitesv6
  4. Minor Study sites: 3 to 13v5
  5. Notable Primary endpoints: 3 to 1v4 Show 7 more changesShow less
    • Enrollment target: 500 to 615
    • Study sites: 4 to 3
    • Secondary endpoints: 11 to 12
    • Study description shortened, about 393 words
    • Publications: 13 to 14
    • Study title revised
    • Eligibility criteria shortened, about 1 word
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  1. Notable Trial status: Not Yet Recruiting to Recruitingv3 Show 4 more changesShow less
    • Primary completion date: Jan 1, 2022 to Jan 1, 2021
    • Study sites: 3 to 4
    • Start date changed from estimate of Apr 1, 2018 to Feb 20, 2018
    • Study description expanded, about 18 words
  2. Notable Lead sponsor: Bergman Clinics to Marc Schröder
    • Secondary endpoints: details revised at 4 of 11 entries
    • Study description shortened, about 332 words
    • Publications: 1 to 13
    v2
  1. Minor Study First Submitted
  • Stopped: an ongoing trial was terminated, suspended or withdrawn.
  • Notable: the trial’s plan changed such as a big move in its timeline or size, a new primary endpoint, sponsor or phase, or recruiting opened or resumed.
  • Minor: routine progress and housekeeping, such as sites added or enrollment closed.
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.
Trial Details
NCT Number NCT03398915
Lead Sponsor Marc Schröder
Collaborators: University Hospital, Zürich
Conditions
(from sponsor)
Degenerative Disc Disease, Spondylolisthesis, Spinal Stenosis, Recurrent Disc Herniation, Spondylodiskitis, Spinal Tumor, Spinal Metastases
Related terms Discitis, Intervertebral Disc Degeneration, Intervertebral Disc Displacement, Spinal Cord Neoplasms, Spinal Stenosis, Spondylolisthesis
Enrollment 932 participants
Start Date
Primary Completion (estimated)
Study Completion (estimated)
Updated on ClinicalTrials.gov