Actively Recruiting

Age: 18Years +
All Genders
NCT05915000

CSF Protein Markers as Prognostic Indicators of the Response to CSF Shunt in Normotensive Hydrocephalus

Led by University of Valencia · Updated on 2026-04-22

150

Participants Needed

2

Research Sites

546 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

In all published series of adult chronic hydrocephalus, there is a percentage between twenty and twenty-five percent of patients who present poor results after implantation of a cerebrospinal fluid shunt,1-11 usually ventriculoperitoneal. The lumboperitoneal shunt is also used but much more rarely. The diagnosis of this pathology is based on the clinical picture, neuroimaging studies (Evans index and corpus callosum angle), cerebrospinal fluid dynamics tests (Katzman test), and invasive intracranial pressure measurements. Despite all this diagnostic arsenal, there is a high percentage of patients (mentioned above) in which treatment by diversion of cerebrospinal fluid does not offer the expected results. Traditionally, this has been attributed to chronic adult hydrocephalus being associated with other types of dementia. This may be the case in some patients, and it would be important to predict which patients will not improve or who will improve poorly in the case of insertion of a cerebrospinal fluid shunt.

CONDITIONS

Official Title

CSF Protein Markers as Prognostic Indicators of the Response to CSF Shunt in Normotensive Hydrocephalus

Who Can Participate

Age: 18Years +
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Age 18 years or older
  • Diagnosis compatible with chronic adult hydrocephalus
Not Eligible

You will not qualify if you...

  • Suspected diagnosis other than adult chronic hydrocephalus
  • Cerebrovascular disease
  • Dementia not caused by adult chronic hydrocephalus
  • Alzheimer's disease
  • Parkinson's disease
  • Hereditary degenerative brain disorders such as Huntington's chorea

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Trial Site Locations

Total: 2 locations

1

Hospital General Universitario de Valencia

Valencia, Valencia, Spain, 46015

Actively Recruiting

2

Vicente Vanaclocha

Valencia, Valencia, Spain, 46015

Actively Recruiting

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Research Team

V

Vicente Vanaclocha, Full Professor

CONTACT

C

Clinical Research Support Office

CONTACT

How is the study designed?

Study Type

OBSERVATIONAL

Masking

N/A

Allocation

N/A

Model

N/A

Primary Purpose

N/A

Number of Arms

0

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