Tiny trial aims to perfect brain stimulation timing for Parkinson's
NCT ID NCT07139093
First seen Jun 24, 2026 · Last updated Jul 01, 2026 · Updated 3 times
Summary
This study tests a device that synchronizes two types of brain stimulation — deep brain stimulation (DBS) and transcranial alternating current stimulation (tACS) — in people with Parkinson's disease. Only 2 participants will be enrolled to see if the device can lock the timing of the two stimulations accurately. The goal is purely technical: to confirm the interface works, not to treat symptoms.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- device: synchronized tACS and DBS
- What this could lead to
- If successful, this could enable future studies that explore whether precisely timed brain stimulation improves symptoms in Parkinson's disease.
- What could go wrong
- This is a very early, tiny trial with only 2 participants, focused on testing the equipment, not on treating the disease. It may not lead to any direct benefit for patients.
This is an AI summary of the original study and may miss details. Read our disclaimer.
Study facts
What this study's own registry entry says, in plain language.
- Phase
-
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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2 people
The number who actually took part.
- Started
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Sep 2025
- Finished
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Feb 2026
- Lead sponsor
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Other sponsor
The registry's catch-all category, for sponsors it does not file as a company, a government agency, or a research network.
Who can take part
This study's own entry requirements. Only the study team can say for certain whether you qualify.
- Ages
-
35 to 85 years
- Sex
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Anyone
- Healthy volunteers
-
Not accepted
This study is not open to healthy volunteers. The entry requirements below say who it is open to.
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Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.
Inclusion Criteria: * Provision of written informed consent by the patient * Age 35 - 85 * patient groups: Parkinson's disease, essential tremor, dystonia * \>3 months after surgery for DBS Exclusion Criteria: * Epilepsy or history of seizures * Existence of heart pacemaker or other metal implants in the body (except DBS) * Pregnancy
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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
-
University Medical Center Hamburg-Eppendorf
Hamburg, 20246, Germany
More trials for these conditions
Other studies related to the condition(s) this trial covers.
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- Brain surgery for Parkinson's: can we foresee the confusion that follows?