New study aims to take the guesswork out of brain surgery for walking problems
NCT ID NCT02495610
First seen Jun 27, 2026 · Last updated Jun 27, 2026
Summary
This study looked at 70 people with idiopathic normal pressure hydrocephalus (iNPH), a condition that causes walking problems, memory loss, and bladder control issues. The goal was to find better ways to predict which patients would benefit from a surgery that drains extra fluid from the brain. Researchers tested walking, thinking, and bladder function before and after a spinal tap to see if those tests could accurately forecast surgery outcomes.
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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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About 70 people
The number the study aims to enrol. It can still change while the study runs.
- Start date
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Jun 2015
- Finished
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Dec 2024
- 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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50 to 85 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.
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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: * Informed consent. * Age 50 years or above * Impaired walking function for at least 3 months, onset at/ after 40 years of age. * MRI or CT with enlarged ventricular system (Evans' index ≥0.30) without evidence of moderate or severe cortical atrophy. * Eligible for shunt surgery. * Eligible for analysis of gait, neuropsychological and urological function. * Subjects must be able to understand the patient information sheet and comply with the requirements of the protocol. Exclusion Criteria: * Previous intracranial disorder or surgery. * Contraindications to surgery or MRI * Contraindications to the testing of gait, bladder or neuropsychological function. * Presence of concomitant disease which might reasonably account for the clinical symptoms or radiological findings. * Worsening of walking function secondary to any other condition occurring during 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.
Contacts and locations
Locations
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University Hospital
Zurich, Canton of Zurich, 8091, Switzerland
More trials for these conditions
Other studies related to the condition(s) this trial covers.
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