Deep Brain Stimulation (DBS) Retrospective Outcomes Study (NCT03664609)
🩺 Plain-English Summary (8th-Grade Level)
The primary objective of this study is to characterize real-world clinical outcomes of Deep Brain Stimulation (DBS) using retrospective review of de-identified patient records.
Who can join: To join this study, participants generally need to meet the listed inclusion criteria (1 items) and avoid the listed exclusions (2 items).
Location: St. Joseph's Hospital & Medical Center — Phoenix, Arizona
🧪 Interventions in This Study
📋 "Do I Qualify?" — 1-Minute Self Screener
Instant ChecklistCheck every box below. If you can check all of them, you may meet the study's basic screening requirements (final eligibility is confirmed by the site team).
Usually NOT eligible if any of the following apply:
- Exclusion Criteria:
- No Exclusion Criteria
🔍 Extracted verbatim from the official NIH eligibility criteria. Always confirm with the study coordinator.
📍 All Participating Trial Locations (19 Sites)
- St. Joseph's Hospital & Medical Center — Phoenix, Arizona
- University of California, San Francisco — San Francisco, California
- University of Miami Hospital — Miami, Florida
- University of South Florida — Tampa, Florida
- St. Luke's Regional Medical Center — Boise, Idaho
- Albany Medical Center — Albany, New York
- Wake Forest University School of Medicine — Winston-Salem, North Carolina
- Allegheny General Hospital — Pittsburgh, Pennsylvania
- Swedish Neuroscience Institute — Seattle, Washington
- AZ St. Lucas — Ghent,
- AZ Delta — Roeselare,
- Hopital Fondation Adolphe de Rothschild — Paris,
- Uniklinik Köln — Cologne,
- Universitaetsklinikum Dusseldorf — Düsseldorf,
- Uniklinikum Jena — Jena,
- Universitaetsklinikum Schleswig-Holstein — Lübeck,
- Universitaetsklinikum Wuerzburg — Würzburg,
- Fondazione Istituto Neurologico Casimiro Mondino — Pavia,
- Hospital Virgen Del Rocio — Seville,
📞 Contact the Study Coordinator
Phone: (855) 213-9890
Email: BSNClinicalTrials@bsci.com
Coordinator details come directly from the registered NIH protocol. Confirm the study is still recruiting before traveling.
💰 Cost, Insurance & Patient Rights
- 100% Free Items: The investigational treatment and protocol-required procedures are supplied at zero cost by the sponsor.
- Routine Patient Care: Under federal law (ACA § 2709) and many state statutes, routine care costs are covered during participation.
- Voluntary Participation: You may withdraw at any time without affecting your standard medical care.
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💡 How to Participate
- Check the checklist above to see if you may qualify.
- Contact the study coordinator using the phone/email above.
- Ask about the visit schedule, what is covered at no cost, and any travel support.
- Confirm with your own doctor before making a decision.