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Hydrocephalus, Normal Pressure clinical trials

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NCT ID: NCT01850914 Completed - Vascular Diseases Clinical Trials

Vascular Risk Factors in INPH-patients

Start date: January 2010
Phase: N/A
Study type: Observational

Idiopathic normal pressure hydrocephalus (INPH) is a treatable and a common disease of the elderly. The overall objective of this work is to describe cardio- and cerebrovascular risk factors and vascular disease in shunted INPH-patients compared to an age- and sex matched elderly population, as well as the impact of vascular risk factors and vascular co-morbidity on clinical symptoms and outcome of surgery in INPH-patients. The hypothesis is that INPH-patients have a higher level of vascular risk factors and subclinical organ damage than a normal elderly population, and that the higher the level of existing vascular risk factors, the more severe the symptoms of the hydrocephalic disease.

NCT ID: NCT01834625 Terminated - Clinical trials for Normal Pressure Hydrocephalus Patients

Prognostic Value of Aβ Imaging in NPH Prior to Shunt Placement

Start date: April 2013
Phase:
Study type: Observational

In this pilot study the investigators shall prospectively in a blinded fashion evaluate with Aβ PET in patients committed to shunt surgery and then investigate the relationship of these biomarkers with outcome on gait, cognition and urinary control improvement in the short term (3 months) and long term (1 year). The imaging agent will be provided by AVID. Furthermore the study will standardize imaging studies using florbetapir F 18 PET to provide information on amyloid burden.

NCT ID: NCT01815775 Completed - Clinical trials for Normal Pressure Hydrocephalus

Predictive Value of Flow MRI in Normal Pressure Hydrocephalus Surgery

Start date: March 2006
Phase: Phase 0
Study type: Interventional

The idea is to assess the predictive value of flow magnetic resonance imaging (flow MRI) for patient suffering normal pressure hydrocephalus (NPH) planned for surgery. By now, the depletive lumbar puncture is the best test assessing the efficacy of a forthcoming surgery. The idea is to demonstrate that flow MRI can be as effective as lumbar puncture in term of predictive value of surgery response. In that way, cerebrospinal fluid (CSF) dynamics are evaluated by a single non invasive examination. CSF flow is measured at the Sylvius' aqueduct, cervical, arachnoid space and 4th ventricle levels.

NCT ID: NCT01798641 Completed - Clinical trials for Normal Pressure Hydrocephalus

A Randomized Cross-over Study for Normal Pressure Hydrocephalus

ARCS NPH
Start date: January 2013
Phase: N/A
Study type: Interventional

The goal of our study is to verify the effectiveness of the shunt and to identify the most sensitive criteria to select patients for surgery. The study is designed to assess improvement in walking and balance (gait), urinary function and memory after shunting. In addition, the study aims to identify the most accurate and sensitive tools to measure improvement for our patients.

NCT ID: NCT01618500 Recruiting - Clinical trials for Normal Pressure Hydrocephalus

Computerised Testing of Cognitive Response to Cerebrospinal Fluid Shunting in Idiopathic Normal Pressure Hydrocephalus

Start date: January 2012
Phase: N/A
Study type: Observational

A novel computerised neuropsychological test battery for normal pressure hydrocephalus (NPH) has been developed. The aim is to provide the clinician with a free of charge, standardized tool, assessing the cognitive decline or improvements in the cognitive domains specific for NPH. Results from the battery indicate good reliability and validity for the computerized tests Results from the computerised battery seems promising. However, ability for the battery to detect cognitive improvements after a shunt operation remains to be tested. Study objectives 1. Improvement after shunt. The aim of this study is to evaluate the effects of shunting on neuropsychological performance in NPH patients, using a computerized battery. 2. Feasibility. The ability to complete the test battery by the intended patient group will be tested. 3. Baseline profile. Baseline scores for NPH-patients will be compared to scores of healthy individuals (from previous study).

NCT ID: NCT01570257 Completed - Clinical trials for Idiopathic Normal Pressure Hydrocephalus

A Trial of High and Low Pressure Level Settings on a Programmable Ventriculoperitoneal Shunt Valve for Idiopathic Normal Pressure Hydrocephalus

Start date: September 2003
Phase: N/A
Study type: Interventional

In treating idiopathic normal pressure hydrocephalus with a shunt there is always a risk of underdrainage or overdrainage. The hypothesis is tested whether treatment of patients with an adjustable valve preset at the highest opening pressure (OPV), leads to comparable clinical results with less subdural effusions than in a control group with an opening pressure preset and kept fixed at a low pressure level.

NCT ID: NCT01374048 Completed - Clinical trials for Idiopathic Normal Pressure Hydrocephalus

Intracranial Pressure Waves Via Lumbar Puncture

Start date: n/a
Phase: N/A
Study type: Observational

Patients are subjected to simultaneous intracranial and lumbar puncture pressure measurements. This study focus on intracranial pulse amplitude. Hypothesis: Intracranial pressure amplitude is reflected by lumbar puncture pressure amplitude.

NCT ID: NCT01319136 Completed - Clinical trials for Idiopathic Normal Pressure Hydrocephalus

Improved Analysis Methods for Infusion Tests

Start date: March 2009
Phase: N/A
Study type: Observational

Objective: Patients with Idiopathic Normal Pressure Hydrocephalus are improved with shunt surgery. To increase the accuracy of the diagnosis, supplementary tests that characterize the cerebrospinal fluid (CSF) dynamics are used. The infusion test is one of these, used for shunt surgery selection and postoperative evaluation of shunt function. Forty-eight patients that had a preoperative investigation because of communicating hydrocephalus at the university hospitals in Umeå and Uppsala, Sweden, participated in the study. The purpose of this study was to evaluate a new method, with a new infusion protocol and new analysis methods, and compare it to the current method.

NCT ID: NCT01265251 Completed - Clinical trials for Normal Pressure Hydrocephalus

Computerized Neuropsychology in Idiopathic Normal Pressure Hydrocephalus (INPH)

Start date: August 2007
Phase: N/A
Study type: Observational

A computerised neuropsychological test battery to be used as a standardised tool assessing the cognitive domains affected by idiopathic normal pressure hydrocephalus INPH was developed. The aim of this study is to investigate the reliability, validity and feasibility of the battery.

NCT ID: NCT01115270 Completed - Clinical trials for Hydrocephalus, Normal Pressure

A Study Comparing Shunt Placement Versus Endoscopic Third Ventriculostomy in the Treatment of Hydrocephalus

Start date: February 2007
Phase: N/A
Study type: Observational

The main purpose of this study is to compare two types of treatment of hydrocephalus: placement of a ventriculoperitoneal (VP) shunt versus an endoscopic third ventriculostomy (ETV). A second goal of this study will be to understand how the two different types of procedures, VP shunt versus ETV, affect brain blood flow and pressures. Understanding these changes is important because the investigators hope is to someday be able to predict who will better respond to one procedure or another.