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Spinal Deformity Outcomes Database Registry

Clinical Trial Title: 
Prospective, multi-center minimally invasive versus open adult spinal deformity outcomes database registry.
Clinical Trial Protocol ID: 
Clinical Trial Investigator Name: 
Richard Fessler, MD, PhD
Clinical Trial Protocol Description: 

To compare outcomes based on application of surgical technique (open, hybrid, circumferential MIS).

The data collected from each site will include chart and radiographic review at the following visits: baseline/preop, 6wk followup, 1yr followup, 2yr followup, and 3-5yr followup.

The case report forms to be utilized for the purpose of collecting specific data and will not contain patient identifiable information.

Clinical Trial Eligibility Criteria: 

In order to participate you must meet the following criteria:

  • Complete signed consent.
  • Complete preoperative data.
  • Undergo surgical treatment (mandatory).
  • Complete surgical data.
  • Complete 6 weeks postoperative data.

This is a partial list of eligibility requirements. To inquire about your eligibility, please call the contact number provided. If you wish to inquire via email, please include the title of the study in your message.

Clinical Trial Area: 
Spine and Back Disorders
Contact Email: 
Contact Phone: 
(312) 942-6570
Contact Name: 
Ewa Gliwa