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Registry Tracking Outcomes of Deep Brain Stimulation in Parkinson's Disease

Records outcomes of deep brain stimulation with a device in adults with Parkinson's disease.

Plain-language title generated from the registry record
Registry title: Registry of Deep Brain Stimulation With the VERCISE™ System: Vercise DBS Registry

Key facts

Where
Bydgoszcz, Gdansk, and Warsaw, PolandSee the 3 sites

Where in Poland

  • 10 Military Clinical Hospital BydgoszczBydgoszcz, PolandNo longer taking part
  • Podmiot Leczniczy Copernicus Sp. z o.o.Gdansk, PolandNo longer taking part
  • Centrum Onkologii Instytut im.Marii Sklodowskiej-CurieWarsaw, PolandNo longer taking part

Questions to ask the study team

  1. How often do I need to come in, and for how long each time?
  2. Are travel costs paid?
  3. Can I keep my own doctor?
  4. What happens if I want to stop?
Print a page for my doctor

Trial details

Who runs it
Boston Scientific Corporation
Trial code
NCT02071134
Record updated
13 October 2026
Original description
The purpose of this registry is to compile characteristics of world-wide outcomes for the use of Boston Scientific's commercially available Vercise DBS System in the treatment of Parkinson's disease.Read full original descriptionShow less

Registry of Deep Brain Stimulation With the VERCISE™ System: Vercise DBS Registry

The purpose of this registry is to compile characteristics of world-wide outcomes for the use of Boston Scientific's commercially available Vercise DBS System in the treatment of Parkinson's disease.

The utilization of Image Guided Programming (IGP), and other commercially available programming features, used as planning tools for the programming of patients with Boston Scientific's Vercise DBS System are also evaluated.

Additionally, the utilization of the DBS Illumina 3D feature that may be used for the programming of patients with Boston Scientific's Vercise DBS Systems is also evaluated.

Inclusion: Meets criteria established in locally applicable Vercise System Direction for Use; At least 18 years old.

Exclusion: Meets any contraindication in the Vercise System locally applicable Directions for Use; Subjects with significant cognitive or psychiatric impairment may be excluded in the evaluation of GXT.

ClinicalTrials.gov NCT02071134

Under construction, not live – Registry of Deep Brain Stimulation With the VERCISE™ System: Vercise DBS Registry (NCT02071134) – Frontlight Research