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Evaluation of Safety of Complex Pedicle Screw Trajectories Using Patient-Specific Guides (MySpine, Medacta)

Retrospective Assessment of the Safety and Accuracy of Pedicle Screw Placement Using Patient-Specific Guides (MySpine, Medacta): Standard Versus Anatomically Complex ("Red Screw") Trajectories

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT07790068
Acronym
Red Screws
Enrollment
130
Registered
2026-08-27
Start date
2026-05-15
Completion date
2026-12-31
Last updated
2026-08-27

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Adult Scoliosis, Adult Spinal Deformity, Scheuermann Disease, Scheuermann's Kyphosis, Scoliosis Associated With Other Conditions, Scoliosis Idiopathic, Scoliosis Idiopathic Adolescent, Scoliosis Idiopathic Adolescent Treatment

Keywords

MySpine, Complex trajectory screws, Adult sagittal deformity, Idiopatic scoliosis, Congenital, syndromic and neuromuscolar spinal deformity

Brief summary

This retrospective, single-center observational study evaluates the clinical safety and neurophysiological performance of patient-specific MySpine guides (Medacta International) for pedicle screw placement in patients undergoing instrumented spinal surgery. Particular attention is focused on anatomically complex trajectories identified during preoperative planning as "Red Screws," in which complete osseous containment of the planned screw trajectory cannot be ensured because of dysplastic, hypoplastic, or otherwise challenging pedicle anatomy. The study includes 130 patients treated between January 2015 and January 2026, encompassing a total of 2,626 pedicle screws. The primary objective is to compare the incidence of positive triggered electromyography responses, defined as a stimulation threshold \<8 mA, between standard screws and Red Screws. Secondary objectives are to compare absolute stimulation thresholds, screw-related intraoperative neuromonitoring alerts, the need for screw repositioning or removal, and postoperative neurological deficits considered related to screw placement. An exploratory analysis will also investigate whether a planned medial cortical breach is associated with an increased risk of neurophysiological warning signals or other intraoperative screw-related events.

Interventions

DEVICEPatient-Specific Guides to pedicle screws placement (MySpine, Medacta)

Standard Versus Anatomically Complex ("Red Screw") Trajectories for pedicle screw placement with patient specific guides (MySpine - medacta) in complex deformity cases

Sponsors

I.R.C.C.S Ospedale Galeazzi-Sant'Ambrogio
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
OTHER

Eligibility

Sex/Gender
ALL

Inclusion criteria

* Patients, both adults and minors, who underwent instrumented spinal surgery using MySpine guides at IRCCS Galeazzi - Sant'Ambrogio Hospital between January 1, 2015, and January 31, 2026.

Exclusion criteria

* Incomplete clinical documentation * Procedures performed without using MySpine guides

Design outcomes

Primary

MeasureTime frameDescription
incidence of positive neurophysiological stimulation,Along the surgery time (especially during pedicle screw placement)compare the incidence of positive neurophysiological stimulation, defined as a stimulation threshold below 8 mA, between standard-trajectory screws and "Red Screws."

Countries

Italy

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Aug 28, 2026