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Hydrocephalus clinical trials

View clinical trials related to Hydrocephalus.

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NCT ID: NCT01092546 Terminated - Clinical trials for Normal Pressure Hydrocephalus

Positron Emission Tomography Imaging of Brain Amyloid in Normal Pressure Hydrocephalus

Start date: March 2010
Phase: Phase 3
Study type: Interventional

To determine the level of association between the quantitative estimates of brain uptake of [18F]flutemetamol and the quantitative immunohistochemical and histochemistry estimates of amyloid levels in frontal lobe biopsy samples obtained from subjects during shunt placement for NPH.

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: NCT01041950 Completed - Clinical trials for Intracerebral Hemorrhage

A Randomised Controlled Trial of Lumbar Drainage to Treat Communicating Hydrocephalus After Severe Intraventricular Hemorrhage

LUCAS-IVH
Start date: May 2012
Phase: Phase 2/Phase 3
Study type: Interventional

The purpose of this study is to determine if usage of early lumbar drainage leads to less shunt surgery and less catheter associated complications in patients with communicating hydrocephalus after intracerebral hemorrhage with severe ventricular involvement.

NCT ID: NCT01007786 Completed - Clinical trials for Pediatric Hydrocephalus

The Ventricular Catheter Placement Study: Assessment of Efficacy and Safety of an Ultrasound Guided Shunt Insertion Technique

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

Shunt failure remains a significant problem in pediatric patients with hydrocephalus. If reliable techniques for the accurate placement of ventricular catheters can be developed, shunt survival may improve. The purpose of this study is to assess the efficacy and safety of the ultrasound guided shunt insertion technique in the hands of experienced surgeons. The primary outcome measure is ventricular catheter location determined from post-operative brain images. The study is being conducted by the Hydrocephalus Clinical Research Network (HCRN), a network established to conduct multi-institutional clinical trials on pediatric hydrocephalus. Pediatric neurosurgeons at HCRN centers enrolled in this study will perform either ultrasound guided shunt surgery or a conventional shunt surgery. Patients who undergo conventional shunt surgery will serve as a contemporary control group.

NCT ID: NCT00946127 Terminated - Hydrocephalus Clinical Trials

ETV Versus Shunt Surgery in Normal Pressure Hydrocephalus

Start date: March 2009
Phase: Phase 3
Study type: Observational

The purpose of this study is to test and compare the efficacy of Endoscopic Third Ventriculostomy with shunting of Cerebrospinal fluid (CSF)for treatment for patients of Normal pressure Hydrocephalus.

NCT ID: NCT00886054 Active, not recruiting - Ischemic Stroke Clinical Trials

The Prediction of Intracranial Pressure and Clinical Outcome by Transcranial Doppler in Neurocritical Patients

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

The purpose of this study is to use transcranial Doppler (TCD) to predict intracranial pressure (ICP) and clinical outcome of neurocritical patients.

NCT ID: NCT00875758 Completed - Hydrocephalus Clinical Trials

Optimizing Treatment of Post-hemorrhagic Ventricular Dilation in Preterm Infants

LETAP
Start date: May 2009
Phase: N/A
Study type: Interventional

Intraventricular hemorrhage remains the most frequent, severe neurological complication of prematurity, occurring in 25-30% of preterm infants. Post-hemorrhagic ventricular dilation (PHVD) occurs in 25-50% of those infants, with over half requiring ventriculoperitoneal shunts. When suboptimally untreated, PVHD results in a 3-4 fold increase in neurodevelopmental delay. Despite the lifelong impact of PHVD on quality of life, little research has been done over the past 20 years to improve patient outcomes. The CENTRAL HYPOTHESIS of this project is that early treatment of PHVD will reduce shunt-dependence and improve neurodevelopmental outcome in preterm infants.

NCT ID: NCT00874198 Unknown status - Clinical trials for Normal Pressure Hydrocephalus

European Study on Prediction of Outcome in Patients With Idiopathic Normal Pressure Hydrocephalus

Start date: October 2004
Phase: N/A
Study type: Interventional

The purpose of the study is to determine the predictive values and prognostic accuracies of CSF dynamic measures, the TAP -TEST (high-volume cerebrospinal fluid withdrawal), resistance to CSF outflow and compliance in the prediction of shunt-treatment outcome in patients with idiopathic normal pressure hydrocephalus.

NCT ID: NCT00870675 Completed - Ventriculomegaly Clinical Trials

Magnetic Resonance Imaging (MRI) of Ventriculomegaly: Morphology and Outcome

Start date: January 1996
Phase: N/A
Study type: Observational

This study compares the accuracy of fast magnetic resonance imaging (MRI) using the half Fourier single shot rapid acceleration with relaxation enhancement technique to ultrasound in the diagnosis of fetal abnormalities. The investigators' specific aim is to perform MRI examinations with ultrafast MRI on fetuses with sonographic morphologic abnormalities. The investigators' hypotheses are that 1) MRI will demonstrate fetal morphologic abnormalities; and 2) MRI will add additional information to the sonographic diagnosis which may directly affect maternal and/or neonatal care.

NCT ID: NCT00793416 Withdrawn - Clinical trials for Normal Pressure Hydrocephalus

ShuntCheck Accuracy in Detecting Shunt Obstruction Normal Pressure Hydrocephalus (NPH) Patients

Start date: November 2008
Phase: Phase 4
Study type: Interventional

The purpose of this study is to examine the role of ShuntCheck and MR Imaging in evaluating the presence or absence of Shunt Obstruction in the patients of Hydrocephalus or Idiopathic Intracranial Hypertension (IIH) undergoing radionuclide test for suspected shunt obstruction. This is an exploratory study to determine how a non-invasive device can assist in detection of presence of flow in these patients.