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Study identifier: NCT06827795 Synced from ClinicalTrials.gov · July 29, 2026
● Recruiting

An Open, Parallel-group, Randomized, Medical Device Study to Assess the Usability and Performance of Surgify HaloTM in Spine Surgery Versus State-of-art (Rosen Burr)

Condition: Spine Surgery  ·  Sponsor: Surgify Medical Oy

PhaseNA
Planned participants30
Who can joinAll sexes, 21 Years to 85 Years
Healthy volunteersNo

About this study

The purpose of this research study is to: test the usability and performance of the medical device Surgify Halo ™ in spine surgery test the level of "chattering " during the use of the device test the cutting performance of Surgify Halo™in comparison to the usual drill bit used in spine surgery ( Rosen burr). This medical device is available for its indications for shaping and removal of hard tissue and bone in neurosurgical, spinal, ENT, and general surgical procedures. The target is to enroll 30 participants in this study.

This description comes directly from the study's public registry record.

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Locations (1)

North Shore University HospitalNew York, New York, United StatesRecruiting

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Source record: clinicaltrials.gov/study/NCT06827795