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Clinical Trial Details — Status: Active, not recruiting

Administrative data

NCT number NCT01909960
Other study ID # PHRCIR11-DR-BALEDENT
Secondary ID 2011-A01633-38
Status Active, not recruiting
Phase N/A
First received
Last updated
Start date May 3, 2012
Est. completion date September 2018

Study information

Verified date August 2018
Source Centre Hospitalier Universitaire, Amiens
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

Normal pressure hydrocephalus diagnosis based on quantitative study of cerebro-spinal fluid and blood flow by phase contrast magnetic resonance imaging.


Recruitment information / eligibility

Status Active, not recruiting
Enrollment 144
Est. completion date September 2018
Est. primary completion date September 2018
Accepts healthy volunteers No
Gender All
Age group 18 Years and older
Eligibility Inclusion Criteria:

- Ventricular dilation seen on morphological magnetic resonance imaging (MRI)

- Walking disorder

- Cognitive disorder

- Participants gave their written informed consent

Exclusion Criteria:

- Contra-indication to MRI

- Obstructive tumoral hydrocephalus

- Curatorship or tutorship

- Pregnancy or lactation

- No social assurance

Study Design


Intervention

Other:
Flow imaging
Quantitative flow study was performed by 2D phase-contrast velocity-encoded cine MRI (repetition/echo time, 15/7 ms; field of view = 140 x 140 mm²; matrix size = 256 x 128, flip angle = 25 degrees,one excitation, slice thickness = 5 mm). Cerebrospinal fluid and blood flows are measured with a velocity-encoding value of 5-10 cm/s and 80 cm/s respectively. Peripheral gating was used to cover the entire cardiac cycle with retrospective cardiac synchronization of 32 quantitative flow-encoded images per cycle. Clinical examination consists in Larson's score and MMSE

Locations

Country Name City State
France CHU Amiens Amiens Picardie
France CHU Lille Lille Nord Pas De Calais

Sponsors (1)

Lead Sponsor Collaborator
Centre Hospitalier Universitaire, Amiens

Country where clinical trial is conducted

France, 

Outcome

Type Measure Description Time frame Safety issue
Primary cerebrospinal fluid (CSF) stroke volume evolution other 6 months Measurement of cerebrospinal fluid (CSF) stroke volume via flow MRI at the Sylvius' aqueduct, pontine cistern and spinal spaces levels and determination of its evolution Day 1 (baseline), Day 180
Secondary Blood flow analysis : evolution other 6 months Assessment of arterial (internal carotids and cerebral arteries) and venous (sagittal sinus, straight sinus) blood flow in terms of mean cerebral blood outflow and stroke volume and determination of blood flow evolution. Day 1 (baseline), Day 180
Secondary Larson's score evolution over 6 months Record symptoms on walking, living conditions and urinary disorders Day 1, Day 180
Secondary Neuropsychological test evolution over 6 months Consists in mini mental status evaluation (MMSE) for cognitive evaluation Day1, Day 180
Secondary Blood flow analysis : evolution other one year Assessment of arterial (internal carotids and cerebral arteries) and venous (sagittal sinus, straight sinus) blood flow in terms of mean cerebral blood outflow and stroke volume and determination of blood flow evolution. Day 1 (baseline) and Day 365
Secondary Larson's score evolution over one year Record symptoms on walking, living conditions and urinary disorders Day 1 and Day 365
Secondary Neuropsychological test evolution over one year Consists in mini mental status evaluation (MMSE) for cognitive evaluation Day1, Day 365
Secondary cerebrospinal fluid (CSF) stroke volume evolution other one year Measurement of cerebrospinal fluid (CSF) stroke volume via flow MRI at the Sylvius' aqueduct, pontine cistern and spinal spaces levels and determination of its evolution Day1 (baseline), Day 365
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