Combined Flow and Pressure Study of Craniospinal Dynamic

NCT ID: NCT05068128

Last Updated: 2024-04-10

Basic Information

• Recruitment Status: ACTIVE_NOT_RECRUITING
• Total Enrollment: 73 participants
• Study Classification: OBSERVATIONAL
• Study Start Date: 2021-09-01
• Study Completion Date: 2024-09-30

Brief Summary

Normal pressure hydrocephalus (NPH) can cause a type of dementia. However, this type of dementia is the only one that is reversible. To treat this dementia it is necessary to evacuate the accumulation of CSF from the brain to another body cavity using a device called a shunt. But the implantation of this shunt is only effective when the cause of the pathology is an alteration of the normal circulation of the CSF. To diagnose these patients, morphological MRI and lumbar puncture are standard approaches used but remain perfectible in diagnostic terms.

The main objective is to build a new model of the interaction of intracranial pressures and fluids in order to obtain a new parameter allowing to obtain information on the cerebral biomechanics.

Conditions

Intracranial Pressure; Cerebral Blood Flows; Infusion Test; Phase Contrast MRI; Hydrocephalus; Dementia

Study Design

• Observational Model Type: CASE_ONLY
• Study Time Perspective: PROSPECTIVE

Interventions

Flow MRI

4 flow acquisitions based on the 2D cine phase contrast sequence (present on all MRI systems) will be performed.

This sequence requires a cardiac synchronization by a plethysmograph put on the patient's finger.

32 cardiac phases are reconstructed per acquisition. The processing of the flow MRIs and the analysis of the flow curves of the LCS and blood during the cardiac cycle will be performed using the Amiens software.

Parameters measured via flow MRI are:

• Cerebral vascular flow, intracranial LCS dynamic volume, extracranial LCS dynamic volume

Intervention Type: OTHER

PERFUSION TEST

The test will be performed will include:

• Inserting a needle into the lumbar space, Ommaya reservoir or valve pre-chamber, as appropriate
• Connect the needle to the pressure transducer via saline filled manometer lines connected via a 3-way valve. The other end of the 3-way connection will be connected to a saline
• Recording of the opening pressure for 10 minutes
• The infusion test is terminated either when the pressure stabilizes again on a new plateau, or when the average pressure exceeds 40 mmHg, or in case of adverse effects or symptoms such as headache, nausea/vomiting or visual disturbances.
• At the end of the test, a depletion of 30 to 50 mL of CSF will be performed.
• The pressure recording during the test is then used to calculate the parameters of the mechanical properties of the CSF circulation and reported to the neurosurgeon ordering the test.

Intervention Type: OTHER

Eligibility Criteria

Inclusion Criteria

• age > 55 years
• Patients with suspected active hydrocephalus (HA) known as "normal pressure":
• Ventricular dilatation: Evans index > 0.3
• Patients with cognitive impairment, and/or gait disorders and/or urinary incontinence or a combination of these three symptoms.
• Absence of other neurological diseases that could cause ventriculomegaly.
• Information and collection of the patient's non opposition

Exclusion Criteria

• All patients with neurological disease other than active hydrocephalus will be excluded.
• Individuals who cannot tolerate an MRI examination
• All individuals with implants, pacemakers, prostheses and ferromagnetic objects
• Patients under guardianship, curators or safeguard of justice

• Minimum Eligible Age: 55 Years
• Eligible Sex: ALL
• Accepts Healthy Volunteers: No

Sponsors

University Hospital, Caen

OTHER

Sponsor Role: collaborator

University Hospital, Brest

OTHER

Sponsor Role: collaborator

Centre Hospitalier Universitaire, Amiens

OTHER

Sponsor Role: lead

Responsible Party

Responsibility Role: SPONSOR

Locations

CHU Amiens

Salouël, , France

Countries

France

Other Identifiers

PI2021_843_0017

Identifier Type: -

Identifier Source: org_study_id