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NCT02678429 Clinical Trial

Atlas Predicted DBS Settings in Essential Tremor

Essential Tremor Clinical Trial

Official title:
Atlas Predicted DBS Settings in Essential Tremor

Clinical Trial Details — Status: Terminated

Administrative data
NCT number NCT02678429
Other study ID # 160155
Secondary ID
Status Terminated
Phase N/A
First received
Last updated
Start date September 2016
Est. completion date November 19, 2021

Study information
Verified date March 2023
Source Vanderbilt University Medical Center
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

Programming Deep Brain Stimulation for the treatment of Essential Tremor can be a time intensive process. Using an atlas created using functional tremor responses in the operating room to determine the optimal settings would lead to a faster response for the patient and improved quality of life.

Recruitment information / eligibility
Status Terminated
Enrollment 4
Est. completion date November 19, 2021
Est. primary completion date November 19, 2021
Accepts healthy volunteers No
Gender All
Age group 18 Years and older
Eligibility Inclusion Criteria: Seleced for DBS of the VIM nucleus at Vanderbilt Medical center Diagnosis of essential tremor Exclusion Criteria: Unable to use the patient handheld programmer

Study Design

Related Conditions & MeSH terms

Intervention

Device:
• Change DBS programming
Patient will change their DBS settings to move from one DBS setting to the other, allowed one hour to adjust to the new setting prior to testing

Locations
Country Name City State
United States Vanderbilt University Nashville Tennessee

Sponsors (1)
Lead Sponsor Collaborator
Vanderbilt University

Country where clinical trial is conducted

United States, 

Outcome
Type Measure Description Time frame Safety issue
Primary Fahn-Tolusa-Marsden Tremor Rating Scale Tremor quantification 1 month
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