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Could a simple nerve stimulator ease bladder troubles in Parkinson's?

NCT ID NCT02190851

What the study statuses mean

This study's is highlighted.

Recruitment status, easiest to join first

Recruiting now
This trial is taking on new participants right now.
Not yet recruiting
Registered, but not yet taking participants.
By invitation only
Not open to general applications. Only people the study team invites can take part.
Paused
Paused for now. It may or may not start again.
Ongoing
Running, but no longer taking on new participants.
Completed This study
The trial has finished. Results may not be published yet.
Stopped early
Stopped early, before it reached the end. That can be for many reasons, including safety.
Cancelled
Cancelled before anyone took part.

Expanded access (not trials)

Expanded access
Not a trial. This treatment can be requested outside a study, case by case, for people who qualify.
Expanded access (paused)
Not a trial. The treatment can normally be requested outside a study, but is unavailable right now.
Expanded access (ended)
Not a trial. The treatment could once be requested outside a study, but no longer can.
Approved
The treatment has been approved, so it is available normally rather than through this programme.

When the status isn't known

Details not published
The full record has not been published yet, so there is little to show here.
Status unknown
This status has not been confirmed recently, so it may be out of date.

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

Apr 2015

Finished

Oct 2020

Lead sponsor

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

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

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

  • Hospital Chenevier

    Créteil, 94000, France

  • Hospital Dubos

    Pontoise, 95300, France

  • Hospital Poincare

    Garches, 92380, France

  • Huriez Hospital

    Lille, 59037, France

  • Pontchaillou Hospital

    Rennes, 35, France

  • UHToulouse

    Toulouse, 31059, France

  • Uiversity hospital

    Marseille, 13385, France

  • University Hospital

    Lyon, 69310, France

  • University hospital

    Paris, 75013, France

  • University hospital

    Rouen, 76038, France

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