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Impact of Cerebral Ventricular Dilatations and Cerebrospinal Fluid Pulsations on Periventricular White Matter in Hydrocephalic Patients

Impact of Cerebral Ventricular Dilatations and Cerebrospinal Fluid Pulsations on Periventricular White Matter in Hydrocephalic Patients

Status
UNKNOWN
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT05825521
Acronym
HYDRODIFF
Enrollment
80
Registered
2023-04-24
Start date
2019-12-14
Completion date
2023-12-31
Last updated
2023-04-27

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Cerebral Ventricle, Cerebrospinal Fluid, Hydrocephalus, White Matter Fiber

Keywords

Hydrocephalus, cerebral ventricles, cerebrospinal fluid, white matter fibers, functional biomarkers

Brief summary

Hydrocephalus is characterized by excessive accumulation of cerebrospinal fluid (CSF) in the ventricles of the brain. One of the forms of hydrocephalus is called normal pressure, although one of the main signs is precisely an alteration of the intracranial pressure (ICP), it is here called active hydrocephalus (HA). Although MRI is the reference radiological modality for the characterization of HA. The Evan's and DESH index are radiological diagnostic criteria based on the dilation and morphology of the CSF compartments. These morphological indices remain insensitive and specific. In recent years, advances in Phase Contrast (MRI-PC) and Diffusion (MRI-DTI) MRI have generated new biomarkers of brain viability. The aim of this study is to characterize by MRI the impact of hydrocephalus on brain fluids and tissues.

Interventions

OTHERMRI

During management, patients with hydrocephalus will be subjected to flow MRI and diffusion MRI. Flow parameters and diffusion parameters will be measured and compared to those found in control subjects receiving the same type of imaging

Sponsors

Centre Hospitalier Universitaire, Amiens
Lead SponsorOTHER

Study design

Allocation
NON_RANDOMIZED
Intervention model
PARALLEL
Primary purpose
DIAGNOSTIC
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
55 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* For Patients with hydrocephalus: * Age \> 55, * Ventricular dilation: Evans Index \> 0.3; * Patients with cognitive impairment, and gait disturbances and/or urinary incontinence or a combination of these three symptoms; * Absence of other neurological diseases that could cause ventriculomegaly, information and non-opposition. * For Controls: * Age ≥ 55; * No ventricular dilation: Evans Index \< 0.3; * Individuals who have no neurological or psychiatric disease; * No neurological deficit. * No history of neurosurgery or head trauma; * signed informed consent; * affiliation to a social security scheme.

Exclusion criteria

* All patients who have a neurological disease other than active hydrocephalus will be excluded; * Individuals unable to sign or understand consent; * Individuals with psychiatric, neurological or medical development; * Individuals under treatment with psychoactive drugs; * Individuals who cannot tolerate an MRI examination; * Any individual with implant, pacemaker, prosthesis and ferromagnetic object

Design outcomes

Primary

MeasureTime frame
Variation of MRI flow between both groups3 years
Variation of MRI diffusion between both groups3 years

Countries

France

Contacts

Primary ContactOlivier BALEDENT, MD
olivier.baledent@chu-amiens.fr33 3 22 08 95 20

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026