Data Collection Study on Patients Receiving a DRG Stimulator

Clinical Trial Title

A post-approval study to evaluate targeted SCS (DRG) stimulation for the management of moderate to severe chronic, intractable, pain of the lower limbs due to CRPS types I and II.

Contact Information

Clinical Trial Protocol Description:

Research study to collect data on patients who are receiving a DRG stimulator.

Clinical Trial Eligibility Criteria:

In order to participate you must meet the following criteria:

  • Have a DRG stimulator implant scheduled.

You will be excluded from the study if any of the following criteria apply to you:

  • Do not have or are not planning on receiving a DRG stimulator.

This is a partial list of inclusion and exclusion criteria.

Study Details

Clinical Trial Investigator

Timothy R. Lubenow, MD

Contact Information

Sherry Robison

(312) 942-2985

Location

Rush University Medical Center

1620 W Harrison St
Chicago, IL 60612

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