Actively Recruiting
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
Eligibility Criteria
You may qualify if you...
- Age 18 years or older
- Diagnosis compatible with chronic adult hydrocephalus
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
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
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
Not the Right Trial for You?
Explore thousands of other clinical trials that might be a better match.
Sign up to get personalized trial recommendations delivered to your inbox.
Already have an account? Log in here