Spinal Deformity Outcomes Database Registry

Clinical Trial Title

Prospective, multi-center minimally invasive versus open adult spinal deformity outcomes database registry.

National Clinical Trial Number:


Contact Information

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.

Study Details

Clinical Trial Investigator

Richard Fessler, MD, PhD

Contact Information

Ewa Gliwa


RUSH University Medical Center

1620 W Harrison St
Chicago, IL 60612

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