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NCT03501810

Study Assessing Safety and Performance of OrtoWell Distractor in Patients Undergoing Spinal Surgery

Status unknown Last updated 18 April 2018
What this trial tests

trial testing Distractor use for vertebrae separation in Spinal Surgery in 32 participants. Status unknown.

Timeline
5 April 2018
Primary endpoint
31 July 2018
30 September 2018

Quick facts

Lead sponsorOrtoWay AB
StatusStatus unknown
Study typeOBSERVATIONAL
Enrollment32
Start date5 April 2018
Primary completion31 July 2018
Estimated completion30 September 2018
Sites1 location across Germany

Drugs / interventions tested

Conditions studied

Sponsor

OrtoWay AB

Who can join

Adults 18 to 75, any sex, with Spinal Surgery. Patients with the condition only — healthy volunteers not accepted.

Sponsor's own description

Study to Assess the Safety and Performance of the OrtoWell® Distractor in Patients Undergoing Spinal Surgery

Publications & conference data

1 peer-reviewed publication reference this trial (live from Europe PMC):

  1. A Prospective Clinical Study to Evaluate Safety and Performance of an Intra-Surgical Hydraulic Distractor During Spinal Surgeries.
    Bornemann R, Himstedt J, Boszczyk B, Bowald S, et al · · 2025 · PMID 41164796 · DOI 10.2147/mder.s537601

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Other recruiting trials for Spinal Surgery

Currently open trials in the same condition.

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Data sources for this page

Drug Landscape aggregates and links these public records for informational use only. Always verify against the primary source before clinical or regulatory decisions. Canonical URL: https://druglandscape.com/trial/NCT03501810.

Primary sources · FDA · ClinicalTrials.gov · EMA · SEC EDGAR · ChEMBL · Wikidata · full sourcing