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Hydrocephalus clinical trials

View clinical trials related to Hydrocephalus.

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NCT ID: NCT01973764 Terminated - Hydrocephalus Clinical Trials

Intraventricular Drain Insertion: Comparison of Ultrasound-guided and Landmark-based Puncture of the Ventricular System

In-Vent
Start date: November 2013
Phase: N/A
Study type: Interventional

Puncture of the ventricular system is one of the most frequently performed neurosurgical interventions. This procedure is commonly performed in order to treat and/or measure pathologically elevated intracranial pressure.Therefore a safe and fast surgical procedure is needed. Currently the "landmark-based" placement of intraventricular catheters is the gold standard. However it is known that more than 60% of the catheters are not accurately placed in accordance with "landmark-based" procedures. When the catheter is not placed accurately multiple punctures may be required. In this study, the investigators aim to investigate prospectively whether ultrasound guidance leads to a lower number of incorrect catheter placements, and whether this guidance consequently decreases the number of punctures.

NCT ID: NCT01936272 Active, not recruiting - Hydrocephalus Clinical Trials

Randomized Controlled Trial of Shunt vs ETV/CPC for PIH in Ugandan Infants

Start date: May 27, 2013
Phase: Phase 3
Study type: Interventional

Two treatment options exist for infant patients with hydrocephalus. Most patients are treated with a surgical procedure in which a shunt is inserted into the brain and abdomen. In recent years, however, another treatment has developed called Endoscopic Third Ventriculostomy (ETV) with Choroid Plexus Cauterization (ETV/CPC).This research study is being done to measure the results of these procedures in children less than six months of age who have hydrocephalus as the result of a brain infection, called post-infectious hydrocephalus, or PIH. This study will evaluate patients in more detail to measure brain growth and development.

NCT ID: NCT01909960 Active, not recruiting - Clinical trials for Normal Pressure Hydrocephalus

Flow MRI in Normal Pressure Hydrocephalus

HydroFlux
Start date: May 3, 2012
Phase: N/A
Study type: Interventional

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

NCT ID: NCT01885468 Completed - Clinical trials for Hydrocephalus Shunt (proGAV) Requiring Adjustment

X-Ray Verified Accuracy of the proGAV Verification Instrument

X-AMIN
Start date: May 2013
Phase: N/A
Study type: Observational

This study is to verify the use of a hand held tool to verify the new setting of a hydrocephalus shunt (proGAV). This tool would be used in place of an Xray of the patient's head, which is how settings are verified currently.

NCT ID: NCT01878136 Withdrawn - Clinical trials for Subarachnoid Hemorrhage

Effect of Intraventricular tPA Following Aneurysmal Subarachnoid Hemorrhage

Start date: March 2015
Phase: Phase 1/Phase 2
Study type: Interventional

This study will evaluate the hypothesis that the administration of intraventricular tPA reduces the rates of cerebral vasospasm and ventriculoperitoneal shunt-dependent hydrocephalus in patients with aneurysmal subarachnoid hemorrhage.

NCT ID: NCT01865149 Recruiting - Hydrocephalus Clinical Trials

Comparison of Optic Nerve Sheath Diameter on Retrobulbar Ultrasonography Before and After Drainage of Cerebrospinal Fluid in Pediatric Patient With Hydrocephalus

Start date: May 2013
Phase: N/A
Study type: Observational

Studies in patients with intracranial hypertension have shown a good relationship between optic nerve sheath diameter measured by retrobulbar ultrasound and invasively measured intracranial pressure. The aim of this study was to evaluate changes in optic nerve sheath diameter before and after drainage of cerebrospinal fluid in patients with hydrocephalus.

NCT ID: NCT01863381 Terminated - Hydrocephalus Clinical Trials

Comparison of Continuous Non-Invasive and Invasive Intracranial Pressure Measurement

Start date: September 2014
Phase: N/A
Study type: Interventional

This research is being done to determine the accuracy of two noninvasive methods of measuring the pressure of the cerebrospinal fluid (CSF), also known as intracranial pressure or ICP.

NCT ID: NCT01863329 Terminated - Hydrocephalus Clinical Trials

Comparison of Optic Nerve Sheath Diameter on Retrobulbar Ultrasound Before and After Drainage of Cerebrospinal Fluid in Patient With Hydrocephalus

Start date: March 2013
Phase:
Study type: Observational

Studies in patients with intracranial hypertension have shown a good relationship between optic nerve sheath diameter measured by retrobulbar ultrasound and invasively measured intracranial pressure. The aim of this study was to evaluate changes in optic nerve sheath diameter before and after drainage of cerebrospinal fluid in patients with hydrocephalus.

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.