TARGET Study

TARGET study is sponsored by Abbott. TARGET is a post-approval study to evaluate Targeted Spinal Cord Stimulation (DRG) for the management of moderate to severe chronic intractable pain of the lower limbs due to Chronic Regional Pain Syndrome (CRPS) types 1 and 2.
Post-market follow up study to show how well the SCS works.

Primary Investigator: Dr. Michael Esposito

For more info please visit clinicaltrials.gov

DELIVERY Study

DELIVERY study is sponsored by Abbott. The purpose of this research study is to compare 2 implant spinal cord stimulator techniques for the placement of the leads (wires) during the trial evaluation period. In the interest of this study and in order to be able to compare the 2 techniques you will be randomized to one of the 2 different lead placement technique groups.

Primary Investigator: Dr. Michael Esposito

PRESS Study

PRESS study is sponsored by Vertiflex. The purpose of this post-market surveillance is to gather evidence documenting the performance and clinical outcomes associated with the treatment of moderate degenerative lumbar spinal stenosis using Superion Indirect Decompression System (IDS).

Primary Investigator: Dr. Ashish Udeshi

Product Surveillance Registry (PSR)

PSR study is sponsored by Medtronic. The purpose of the Registry is to provide continuing evaluation and periodic reporting of safety and effectiveness of market-released products for their intended use (Spinal cord stimulators and pain pumps).
Sponsor Medtronic

Primary Investigator: Dr. Ashish Udeshi

For more info please visit clinicaltrials.gov

For more study information, please email our Clinical Research Coordinator Thalia Newton at TNewton3@surgerypartners.com. You may also call 321-784-8211 ext 6241125.