Actively Recruiting
Boston Scientific Registry of Deep Brain Stimulations for Treatment of Essential Tremor (ET): ET Registry
Led by Boston Scientific Corporation · Updated on 2026-05-07
500
Participants Needed
20
Research Sites
N/A
Total Duration
On this page
AI-Summary
What this Trial Is About
This research aims to compile information about real-world outcomes for people with Essential Tremor who receive Deep Brain Stimulation (DBS) therapy using Boston Scientific's approved DBS Systems. The study focuses on collecting data to add to existing evidence about this treatment for Essential Tremor. Participants in this observational study are people with Essential Tremor who are implanted with Boston Scientific's Deep Brain Stimulation Systems according to local directions for use. The study observes how these devices are used in typical care settings without assigning treatments. During the study, researchers will track changes in participants' quality of life using a specific questionnaire for Essential Tremor over up to three years. This includes regular assessments to understand how the DBS treatment affects daily living and well-being. The study started in 2019 and will continue through 2029, allowing long-term follow-up of participants.
CONDITIONS
Brief Title
Boston Scientific Registry of Deep Brain Stimulation for Treatment of Essential Tremor (ET)
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Meets criteria established in the locally applicable Directions for Use (DFU) for Essential Tremor
- Is at least 18 years old
You will not qualify if you...
- Meets any contraindication in locally applicable Directions for Use
AI-Screening
AI-Powered Screening
Complete this quick 3-step screening to check your eligibility
Your Study Journey
Duration - 2 to 4 weeks
Participants are screened for eligibility to participate in the trial.
1 visit (in-person)
Duration - Up to 3 years
Participants receive the Deep Brain Stimulation implant for treatment of Essential Tremor.
Approximately 6 post-operative visits
Duration - Up to 3 years
Participants are observed to assess changes in quality of life and other outcomes after implantation.
Annual visits for up to 3 years
Trial Site Locations
Total: 20 locations
1
A.o. LKH Univ.-Kliniken Innsbruck
Innsbruck, Austria
Actively Recruiting
2
AZ Sint-Lucas
Ghent, Belgium
Actively Recruiting
3
UZ Gasthuisberg
Leuven, Belgium
Actively Recruiting
4
AZ Delta
Roeselare, Belgium
Actively Recruiting
5
Vancouver General Hospital
Vancouver, Canada
Actively Recruiting
6
Uniklinik Koln
Cologne, Germany
Actively Recruiting
7
Universitaetsklinikum Dusseldorf
Düsseldorf, Germany
Actively Recruiting
8
Universitaetsklinikum Essen
Essen, Germany
Actively Recruiting
9
Universitatsklinikum Campus Kiel
Kiel, Germany
Actively Recruiting
10
Universitaetsklinikum Giessen und Marburg GmbH
Marburg, Germany
Actively Recruiting
11
Evangelisches Krankenhaus Oldenburg
Oldenburg, Germany
Actively Recruiting
12
Universitaetsklinikum Wuerzburg
Würzburg, Germany
Actively Recruiting
13
Medical School of University PECS
Pécs, Hungary
Actively Recruiting
14
Policlinico Universitario Agostino Gemelli
Rome, Italy
Withdrawn
15
CHU Sao Joao
Porto, Portugal
Actively Recruiting
16
Samsung Medical Center
Seoul, South Korea
Actively Recruiting
17
Seoul ASAN Medical Center
Seoul, South Korea
Withdrawn
18
Yonsei University Severance Hospital
Seoul, South Korea
Actively Recruiting
19
Hospital De Bellvitge
Barcelona, Spain, 30326
Actively Recruiting
20
Hospital General De Asturias
Oviedo, Spain
Actively Recruiting
Research Team
S
Stephanie Delvaux
D
Diane Keesey
How is the study designed?
Study Type
OBSERVATIONAL
Masking
N/A
Allocation
N/A
Model
N/A
Primary Purpose
N/A
Number of Arms
1
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