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Timing of surgery for excess fluid around the brain

Researchers are comparing earlier and later fluid-drainage surgery in people with Parkinson's and normal-pressure hydrocephalus.

Testing a treatment or activity · Study reference: JPRN-UMIN000052904

Plain-language introduction written with AI from the registry; not independently checked by a clinician. Read the original details below ↓

This registry record was last updated over six months ago, or its update date is missing. Recruitment may have changed. Confirm with the team before making plans.

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Results reported

Start (reported date)
2021-05-22
Study finished (reported date)
2025-05-31

Planned dates can move. A study finishing does not tell us when a paper will be published.

Read the results reported in the registry

Changes we have recorded
  • 2026-10-11 — recruiting

These are dates we observed a change, not necessarily the dates it happened.

Papers connected to this study

No connected paper has been found yet. The tracker checks the growing library for study identifiers and registry-linked publications.

Who can join?

Ages 60years-old to 90years-old · Ask the team who can join

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Read all the rules for taking part

Sex eligibility reported by registry: male and female

Inclusion criteria: Patients who have any or all of the following symptoms: gait disturbance, cognitive dysfunction, or urinary dysfunction, and meet the criteria of Evans' index > 0.3, will undergo nuclear medicine examination (head MRI, DaT-SPECT, IMP-SPECT, MIBG myocardial scintigraphy). Patients with disproportionately enlarged subarachnoid-space hydrocephalus (DESH) and gait disturbance should undergo CSF examination. For patients with symptoms of gait disturbance but no DESH, a tap test is performed and cognitive function tests (MMSE: Mini Mental Scale Examination, FAB: Frontal Assessment Battery, TMT: Trail making test), evaluation of urinary dysfunction (I-PSS: International prostate symptom score, OABSS: Overactive bladder symptom score, ICIQ-SF: International Consultation on Incontinence Questionnaire Short Form), evaluation of parkinsonism (Dopa challenging test, MDS UPDRS part III: MDS-Unified Parkinson's Disease Rating Scale part III, iNPHGS: iNPH grading score) are performed before and after (on the day of the tap test, 3 days later, and 7 days later), and if symptoms improve, a diagnosis of normal pressure hydrocephalus is made. Exclusion criteria: Select patients with no pre-existing subarachnoid hemorrhage, meningitis, head trauma, congenital hydrocephalus, or aqueductal stenosis.If the CSF test shows CSF amyloid-beta42 < 500 pg/ml, CSF total tau > 600 pg/ml, and CSF phosphorylated tau > 60 pg/ml, the patient is likely to have Alzheimer's disease and should be excluded.
Full study name & original research details

Official study title

A controlled, randomized, parallel-group, prospective study of lumbar-abdominal shunting for normal pressure hydrocephalus complicated by Parkinson's disease and related disorders. - Shunt-PD study

Short title used by the registry

Random prospective study of lumbar-abdominal shunting for normal pressure hydrocephalus associated with Parkinson's disease.

Original description

Intervention: The randomly selected lumbar-abdominal shunt non-operative group will undergo surgery after 6 months from diagnosis. The randomly selected lumbar-abdominal shunt surgery group will undergo surgery within 3 months of diagnosis. Primary outcome: iNPH grading scale Secondary outcome: 3m up and go, Mini Mental Scale Examination, Frontary Assessment Battery,Trail making Tast, Wechsler Adult Intelligence Scale-Third Edition, Urinary drainage evaluation (urodynamics), Parkinsonnism (Dopa challenging test, MDS-Unified Parkinson's Disease Rating Scale part3)

Conditions reported: Parkinson's disease, Parkinson's disease with dementia, normal pressure hydrocephalus

Registry records for this study

Records are joined using registration identifiers. Titles alone do not establish that two studies are the same.

Study type
Interventional
Interventions
The randomly selected lumbar-abdominal shunt non-operative group will undergo surgery after 6 months from diagnosis. The randomly selected lumbar-abdominal shunt surgery group will undergo surgery within 3 months of diagnosis.
Phases
Not selected
Sponsor
Juntendo University
Start date reported by registry
2021-05-22 (reported)

Registry updated: Not reported · Status last verified by the registry submitter: Not reported

Registry records retrieved 2026-10-11 (UTC). Individual records may have older updates. Recruitment and eligibility must be confirmed with the study team.

Contact the research team

Public study contacts supplied to the registry. Ask whether recruitment is still open and what participation involves.

Tomoyo Shimada · 03-3813-3111 · t-oyamada@juntendo.ac.jp

Study locations

Site status can differ from overall study status. “Status not reported” means local availability needs confirmation. Remote participation and travel arrangements must be checked with the team.

Facility not reported

Japan

Status not reported

The original descriptions and participation rules come from the registry. Participation is voluntary and does not guarantee benefit.