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Hydrocephalus, Normal Pressure clinical trials

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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: 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.

NCT ID: NCT01053312 Completed - Clinical trials for Normal Pressure Hydrocephalus

PET Imaging of Brain Amyloid in Normal Pressure Hydrocephalus

Start date: December 2009
Phase: Phase 3
Study type: Interventional

This study will determine the level of association between the quantitative estimates of brain uptake of [18F]flutemetamol and the quantitative immunohistochemical estimates of amyloid levels in biopsy samples previously obtained during shunt placement in patients who have normal pressure hydrocephalus (NPH).

NCT ID: NCT00600795 Completed - Clinical trials for Normal Pressure Hydrocephalus

Prognostic Value of Transforming Growth Factor-Beta 1 in Normal Pressure Hydrocephalus

Start date: January 2008
Phase: N/A
Study type: Observational

Correlation of cerebrospinal fluid levels of transforming growth factor beta-1 with functional improvements after insertion of ventriculoperitoneal shunt for normal pressure hydrocephalus

NCT ID: NCT00233701 Completed - Clinical trials for Normal Pressure Hydrocephalus

Normal Pressure Hydrocephalus (NPH) Registry

Start date: October 2004
Phase: Phase 4
Study type: Observational

The overall aim of the registry is to develop a longitudinal, observational database that is focused on adult patients with Normal Pressure Hydrocephalus (NPH) that can be used as a source of clinical information for individual surgeons, as well as a national data repository for scientific inquiry and publications.

NCT ID: NCT00221091 Completed - Clinical trials for Idiopathic Normal Pressure Hydrocephalus

Study to Evaluate Efficacy of Shunt Operation for Idiopathic Normal Pressure Hydrocephalus

Start date: September 2004
Phase: Phase 2
Study type: Interventional

This study evaluates the efficacy of shunt operation for idiopathic normal pressure hydrocephalus, and determines the diagnostic value of noninvasive procedures commonly practiced in the clinic.