Could a simple nerve stimulator ease bladder troubles in Parkinson's?
NCT ID NCT02190851
First seen Jun 26, 2026 · Last updated Jun 27, 2026 · Updated 1 time
Summary
This study tested whether a daily 20-minute nerve stimulation (TENS) applied to the ankle could improve bladder control in people with Parkinson's disease or multiple system atrophy. A total of 110 participants used either an active or a sham device for 3 months. The main goal was to see if patients felt their bladder symptoms had improved.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- transcutaneous electrical nerve stimulation (TENS) device
- What this could lead to
- If it works, this could offer a drug-free way to manage bladder symptoms in Parkinson's disease.
- What could go wrong
- This is a small, completed study with no phase designation. The results may not be strong enough to change practice, and the effect could be due to a placebo.
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
-
110 people
The number who actually took part.
- Started
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Apr 2015
- Finished
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Oct 2020
- 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
-
18 to 90 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.
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: * Established diagnosis of Parkinson disease or multisystem atrophy * Refractory lower urinary tract disorders or contra-indications or intolerance to the usual oral treatments * Patient capable of completing the questionnaires * Patient whose written informed consent has been obtained * Patient registered with a social security scheme Exclusion Criteria: * Pregnancy and breast-feeding * Contra-indications to TENS (local skin problems, metal ankle joint replacement, cardiac pacemaker, peripheral neuropathy, subthalamic deep brain stimulation) * Associated neurological disorders (stroke, dementia, multiple sclerosis, spinal cord lesions, peripheral neuropathy) or urological disorders (bladder outlet obstruction, cancer, pelvic organ prolapse, interstitial cystitis) * Unilateral neurological disability * Legally incompetent patient, patient under legal protection * Participation in another study during the present 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.
Contacts and locations
Locations
-
Clinique Saint Augustin
Bordeaux, 33074, France
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Hospital Chenevier
Créteil, 94000, France
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Hospital Dubos
Pontoise, 95300, France
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Hospital Poincare
Garches, 92380, France
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Huriez Hospital
Lille, 59037, France
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Pontchaillou Hospital
Rennes, 35, France
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UHToulouse
Toulouse, 31059, France
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Uiversity hospital
Marseille, 13385, France
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University Hospital
Lyon, 69310, France
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University hospital
Paris, 75013, France
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University hospital
Rouen, 76038, France
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Other studies related to the condition(s) this trial covers.
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