Prospective, Observational Registry of Renaissance-guided Spine Surgeries

Status Terminated

Clinical Trial Summary

To establish an observational registry for systematic collection of clinical data from Renaissance-guided spine surgeries.

Clinical Trial Description

The key objective of this observational registry is to prospectively collect data to facilitate the quantification of potential short- and long-term benefits of Renaissance-guided spine surgery. It establishes a common framework for collaboration between surgeons performing Renaissance-guided spine surgeries in either minimally invasive (MIS) or open surgical approaches.

The main endpoints that will be collected are surgical endpoints (e.g. complication rates), patient reported outcomes (e.g. VAS, ODI), imaging parameters (e.g. coronal and sagittal alignment, mainly in reconstructive surgeries for spinal deformities) and technical parameters (e.g. use of intraoperative fluoroscopy, ratio of planned vs. executed screws). ;

Study Design

Related Conditions & MeSH terms

Clinical Trial Details

NCT number	NCT02212899
Study type	Observational [Patient Registry]
Source	Mazor Robotics
Contact
Status	Terminated
Phase
Start date	February 18, 2015
Completion date	December 30, 2016

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