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Completed

NCT Number: NCT03369158

Pedicle Screw Positioning With MySpine vs Free Hand Technique

Randomized clinical study in order to evaluate the accuracy of pedicle screw positioning during spine surgery performed with MySpine patient match positioning guide or Free hand technique.

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Key information

Conditions

Age range

12 year and older

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

About this study

The proposed study seeks to assess the intraoperative accuracy of the Medacta patient-specific MySpine® pedicle screws placement guides in comparison to free-hand technique.

A pre-operative CT scan of the spine is obtained to create a 3-dimensional model of the patient's spine for the MySpine patient group. This model is then used to preoperatively plan the patient's surgery implantation itself, with the same goals of both free-hand and computer assisted techniques. The theoretical advantage of this technique is accurate implant placement without the added surgical time and complexity of the procedure, with lower radiation exposure thanks to less steps of fluoroscopy checks.

The hypothesis for the present study is that the MySpine® technique can place pedicle screws more accurately in comparison to free-hand technique.

The accuracy of the final implant position with respect to the pre-operative planning will be evaluated through CT post-op analysis.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Patients older than 12 years
  • patients suffering from coronal or sagittal spinal deformities that will undergo a surgical treatment with a posterior approach and pedicle screws placement
  • Patients suitable to undergo spinal stabilization (according to the label indication/contraindications)
  • Patients who are willing and able to provide written informed consent for participation in the study. Written informed consent must be obtained when indication to surgery is confirmed.

Exclusion criteria

  • Patient with congenital spinal deformity (emeverebre, vertebra wedge, vertebrate butterfly, congenital bar, vertebra block)
  • Patients with a previous fusion of the spine in the region where screws will be inserted
  • Patients with any allergy to the device implanted
  • Patients who will be not able to provide their written consent to the study participation
  • Patients who are incapable of understanding and wanting

Treatment and study plan

patient specific pedicle screw positioning guide

Procedure

Other names: MySpine

Free hand technique pedicle screw positioning

Procedure

MUST pedicle screw

Device

Primary outcomes

  1. Accuracy of Pedicle Screw Positioning

    Time frame: 1 week after surgery

    Pedicle screw accuracy is defined as having the entire screw contained within the cortices of each respective pedicle.

Secondary outcomes

  1. Radiological Evaluation of Pedicle Screw Malposition

    Time frame: 1 weeks after surgery

    A CT will be performed before discharge to evaluate the severity of pedicle screws malposition according to Gertzbein in grades 0, A, B or C, with grades 0 or A considered as "safe area.". Level 0 (perfect corrected positioning of the screw), level A (0-2 mm of violation), level B (2-4 mm of violation), level C (˃4mm of violation). The better outcomes correspond to level 0 and the worst to level C.

  2. Occurrence of Malposition Side

    Time frame: 1 weeks after surgery

    Evaluation of malposition on the medial or lateral side

  3. Incidence of Adverse Event

    Time frame: intraoperatively, up to 1 week after surgery

    Occurrence of intra-operative complications reporting

Sponsors and collaborators

Lead sponsor

Medacta International SA

Industry

Registry information

Official study title

A Prospective Clinical Survey on Accuracy of Pedicle Screws Positioning With MySpine Versus Free Hand Technique

Important dates

Study start
2015
Primary completion
2016
Study completion
2017
First posted
Dec 11, 2017
Registry last updated
Sep 2, 2020

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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