Could zapping the spine steady blood pressure in Parkinson's?
NCT ID NCT07322458
First seen Jun 27, 2026 · Last updated Jun 27, 2026
Summary
This study tests whether spinal cord stimulation can help people with Parkinson's disease who experience sudden drops in blood pressure when standing up. Forty participants will receive either an implanted stimulator or a non-invasive version. The goal is to see if the treatment can stabilize blood pressure and improve symptoms over two years.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- spinal cord stimulation (implanted or non-invasive device)
- What this could lead to
- If it works, this could offer a new non-drug option to manage dangerous blood pressure drops in Parkinson's patients, reducing falls and improving daily life.
- What could go wrong
- This is a small, early-stage study with only 40 participants. The effects may be modest or not last long, and the implanted device carries surgical risks.
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
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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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About 40 people
The number the study aims to enrol. It can still change while the study runs.
- Expected to start
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Jan 2026
An estimate. Start dates often move.
- Expected to finish
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Jun 2028
An estimate. End dates often move.
- 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
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40 to 80 years
- 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.
Inclusion Criteria: * 1\. Aged between 40 and 80 years; * 2\. No dementia as measured by the cMMSE scale (formal cMMSE score should be \>20 for subjects with 1 to 6 years of formal education; cMMSE score should be \>24 for subjects with \>6 years of formal education); * 3\. Able and willing to follow instruction of the researcher; * 4\. No other conditions that the researchers consider inappropriate for inclusion: Exclusion Criteria: * 1\. Severe depression (HAMD-17 above 17 as moderate to severe) or anxiety; * 2\. Pregnancy; * 3\. History of alcoholism; * 4\. No skin abnormalities; * 5\. Non-neurological disease-related symptoms that prevent patients from participation in the study.
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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.
How to take part
Only the study team decides who joins. These are the ways to reach them.
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The places running it
1 site. The list below names each one and where it is.
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The official record
ClinicalTrials.gov lists the study team's own contact details, including names and phone numbers. We don't republish those.
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A doctor treating you
A doctor who knows your case can contact a study site on your behalf, and can tell you whether this study is worth pursuing at all.
Contacts and locations
Locations
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Department of Neurology and Institute of Neurology, Ruijin Hospital, Shanghai Jiao Tong University School of Medicine, Shanghai, Shanghai 200025 Recruiting
Shanghai, Shanghai Municipality, China
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