New brain pacemaker programming shows promise for Parkinson's relief
NCT ID NCT03732898
First seen Jun 27, 2026 · Last updated Jun 27, 2026
Summary
This study tested a new way to program deep brain stimulation (DBS) in 15 people with Parkinson's disease. The goal was to see if this different programming pattern could improve their quality of life. Participants already had DBS devices implanted and were monitored for changes in symptoms and daily function.
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Study facts
What this study's own registry entry says, in plain language.
- Phase
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Not a phased trial
Phase numbers describe drug development. The registry uses this when they do not apply, as it does for trials of devices, procedures or behaviour changes, and for observational studies.
- Participants
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15 people
The number who actually took part.
- Started
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Jan 2019
- Finished
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Nov 2025
- Lead sponsor
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A company
The lead sponsor is a pharmaceutical, biotech, or medical-device company.
Who can take part
This study's own entry requirements. Only the study team can say for certain whether you qualify.
- Ages
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Children (under 18), adults (18 to 64) and older adults (65 and over)
- Sex
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Anyone
- Healthy volunteers
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Not accepted
This study is not open to healthy volunteers. The entry requirements below say who it is open to.
Show the full entry requirements Hide the full entry requirements
Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.
Key Inclusion Criteria: 1. Subject with PD implanted bilaterally in the STN and receiving DBS therapy for at least 3 months. 2. Tolerates \> 12 hours OFF medication and, per clinical judgment, be able to perform all study related procedures. 3. Able to understand the study requirements and the treatment procedures and must provide written informed consent before any study-specific tests or procedures are performed. Key Exclusion Criteria: 1. Exhibits significant psychiatric problems, including unrelated clinically significant depression as determined by the investigator. 2. A female who is pregnant, is breastfeeding, or is of childbearing potential and planning to get pregnant
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Conditions
The condition(s) this trial relates to.
As listed by the trial registrant
The condition terms exactly as the trial's registrant entered them.
Contacts and locations
Locations
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Universitaetsklinikum Wuerzburg
Würzburg, Germany
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University Berlin, Charite Virchow
Berlin, Germany
More trials for these conditions
Other studies related to the condition(s) this trial covers.
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