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NCT02684045

Retrospective Chart Review to Assess Outcomes in Subjects That Received MAGNIFUSE® in the Posterolateral Lumbar Spine

Completed Last updated 21 August 2017
What this trial tests

trial in Subjects Received MAGNIFUSE in Posterolateral Lumbar Spine in 76 participants. Completed in 15 August 2017.

Timeline
1 March 2017
Primary endpoint
15 August 2017
15 August 2017

Quick facts

Lead sponsorMedtronic Spinal and Biologics
StatusCompleted
Study typeOBSERVATIONAL
Enrollment76
Start date1 March 2017
Primary completion15 August 2017
Estimated completion15 August 2017
Sites2 locations across United States

Conditions studied

Sponsor

Medtronic Spinal and Biologics — full company profile →

Who can join

Eligibility, any sex, with Subjects Received MAGNIFUSE in Posterolateral Lumbar Spine. Patients with the condition only — healthy volunteers not accepted.

Sponsor's own description

The purpose of this chart review is to assess outcomes in subjects that received MAGNIFUSE in the posterolateral lumbar spine at 1 or 2 continuous levels from L1-S1.

Publications & conference data

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

  1. Allografts and Spinal Fusion.
    Cohen JD, Kanim LE, Tronits AJ, Bae HW. · · 2021 · cited 14× · PMID 34376497 · DOI 10.14444/8056

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Other Medtronic Spinal and Biologics trials

Trials by the same sponsor.

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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/NCT02684045.

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