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

Conditions

• Parkinson's Disease

Eligibility Criteria

Sex

ALL

Age

18 Years - N/A

Healthy Volunteers

Not accepted

Interventions

• Deep Brain Stimulation (DBS) — DEVICE
  Subjects receiving Deep Brain Stimulation (DBS) for the treatment of their Parkinson's disease symptoms will be offered participation in this registry.

Study Details

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.

Key Dates

Start date

Mar 4, 2014

Status verified

May 2026

Primary completion

Dec 31, 2038

Completion

Dec 31, 2038

Study Design

Enrollment

1,500 participants (estimated)

Arms

• Arm: Parkinson's disease
  Subjects with Parkinson's disease who will receive Vercise DBS for deep brain stimulation.

Primary Outcome Measure

Improvement in patient's quality of life (QoL) during the study as compared with baseline [ Time Frame: up to 3 years ]

Central Contacts

• Heleen Scholtes
  855-213-9890
  [email protected]
• Alison Lewis
  855-213-9890
  [email protected]

Locations (28)

Find similar trials in Aliso Viejo, CA

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