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Hydrocephalus clinical trials

View clinical trials related to Hydrocephalus.

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NCT ID: NCT03230032 Completed - Thrombosis Clinical Trials

Pacifier Activated Device and Mother's Voice in Infants at High-risk for Cerebral Palsy

Start date: June 9, 2017
Phase: N/A
Study type: Interventional

The study seeks to determine the efficacy of non-nutritive suck (NNS) training using a pacifier-activated device (PAM) with mothers' voice to condition suck-strength and rhythmicity, in improving the feeding and developmental outcomes of infants at high-risk for CP.

NCT ID: NCT03113799 Completed - Hydrocephalus Clinical Trials

A Study Evaluate Aqueduct's Smart External Drain

SED
Start date: April 12, 2017
Phase: N/A
Study type: Interventional

To evaluate the performance characteristics of the Smart External Drain (SED) compared with standard EVD drains in the hospital setting, specifically: - Number, type and duration of staff interactions. - Regulating and controlling ICP and CSF drainage. - Maintaining system control with patient movement.

NCT ID: NCT03092804 Recruiting - Clinical trials for Normal Pressure Hydrocephalus

The Brain Structure and Neural Network Changing the Before and After Ventriculo-peritoneal Shunting in the Normal Pressure Hydrocephalus Patients

Start date: August 1, 2016
Phase: N/A
Study type: Observational

With the advent of the aging society, dementia becomes the focus of common people. As for the neurodegeneration dementia, no disease modifying treatments have been discovered. Idiopathic normal pressure hydrocephalus (iNPH) is considered as one of reversible dementia, which can be hint by the surgery. In addition, dementia of iNPH is the typical subcortical dementia. Therefore exploring the pathogenic mechanism is conducive to the early diagnosis and treatment. This research is to monitor the changing of iNPHGS, cognitive function, walking ability as well as brain construction imaging and neural network before and after ventriculo-peritoneal shunting in order to demonstrate the pathogenesis of triads. In the process, the supplementary test, for instance, CSF tap test, will be validated the predictive value.

NCT ID: NCT03076723 Terminated - Clinical trials for Hydrocephalus, Normal Pressure

Using Cerebrospinal Fluid Dynamics to Optimize Treatment of Idiopathic Normal Pressure Hydrocephalus

PULSE-OPT
Start date: June 13, 2017
Phase: N/A
Study type: Interventional

The purpose of the study is to determine if the so called pulsatility curve, which describes the relationship between intracranial pressure (ICP) and ICP pulsatility, can be used to predict outcome of treatment, in the form of shunt surgery, in idiopathic normal pressure hydrocephalus (INPH) and to guide the adjustment of shunt opening pressure after the surgery. The main hypotheses of the study are: 1. The pulsatility curve may be the best auxiliary test to predict shunt surgery outcome in INPH patients. With a "fixed" shunt opening pressure, the preoperatively assessed potential pulse amplitude reduction (determined by analysis of the pulsatility curve) predicts postoperative improvement in gait velocity and cognitive functions. 2. A postoperative pulsatility curve can be used to further optimize ICP pulsatility by guiding opening pressure adjustment. Shunt adjustment based on the pulsatility curve three months postoperatively will increase improvement, but not complications, compared to a shunt with "fixed" opening pressure. Based on these hypotheses, three specific aims for the study have been defined: 1. To determine if improvement three month after surgery is associated with postoperative reduction in pulse amplitude. 2. To determine if a pulsatility curve obtained preoperatively can predict improvement in gait velocity and cognitive functions in INPH patients three months after surgery. 3. To compare outcome six months after surgery and complications rates between INPH patients with a "fixed" opening pressure versus those where the shunt has been adjusted based on the pulsatility curve, three months after the shunt insertion.

NCT ID: NCT03061045 Withdrawn - Clinical trials for Neonatal Post-Hemorrhagic Hydrocephalus

Contrast Enhanced Ultrasound Evaluation of Brain Perfusion in Neonatal Post-Hemorrhagic Hydrocephalus

Start date: April 1, 2017
Phase: Phase 4
Study type: Interventional

The aim of the proposed project is therefore to utilize the CEUS technique to assess cerebral perfusion changes before and after ventricular shunting in neonatal cases of PHH. The expectation of the proposed project is to validate statistically significant cerebral perfusion differences before and after shunting in neonates with PHH, as a preliminary feasibility study prior to conducting a large scale, prospective clinical trial incorporating therapeutic interventions using the CEUS technique.

NCT ID: NCT02988154 Recruiting - Hydrocephalus Clinical Trials

Simulation Efficacy in Neurosurgical Education

SENSE
Start date: June 2016
Phase: N/A
Study type: Observational

This study aims to investigate the efficacy of simulation in neurosurgical training.

NCT ID: NCT02900222 Terminated - Hydrocephalus Clinical Trials

Study of Choroid Plexus Cauterization in Patients With Hydrocephalus

Start date: September 1, 2016
Phase: N/A
Study type: Interventional

The purpose of this study is to determine whether endoscopic choroid plexus coagulation is safe in adult patients with communicating hydrocephalus and risk factors for complications from the standard surgical treatment. It may also help determine whether the endoscopic choroid plexus coagulation is effective in treating your communicating hydrocephalus. The Investigators hope that this research will allow us to place fewer shunts in patients with conditions similar to yours, avoiding complications.

NCT ID: NCT02775669 Enrolling by invitation - Hydrocephalus Clinical Trials

Non-invasive Epicutaneous Transfontanel Intracranial Pressure Monitoring in Children Under the Age of One: a Novel Technique

Start date: January 2015
Phase: N/A
Study type: Observational

Investigators compare the ICP of two standard Spiegelberg ICP-probes in children, which underwent an operation due to craniosynostosis.

NCT ID: NCT02775136 Unknown status - Brain Injuries Clinical Trials

An Evaluation of a Non-invasive Brain Monitor

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

HS-1000 device, a proprietary new non-invasive brain monitor, is expected to safely and accurately monitor physiological signs of the brain with minimal discomfort to patients, providing information about normal or abnormal brain-related conditions and providing decision-making support for physicians. Investigators hypothesis that the HS-1000 is capable of detecting and monitoring various neuropathologies, using the acoustic raw data derived from the noninvasive procedure.

NCT ID: NCT02773888 Suspended - Stroke Clinical Trials

An Evaluation of Non-Invasive ICP Monitoring in Patients Undergoing Invasive ICP Monitoring Via an Intraparenchymal Pressure Monitoring Device

Start date: December 2015
Phase: N/A
Study type: Interventional

Invasive intracranial pressure (ICP) monitoring is highly effective, but involves risks. HS-1000 measures ICP non-invasively by assessing the acoustic properties of the patient's head. HS-1000 device, a proprietary non-invasive ICP monitor, is expected to safely and accurately monitor ICP with minimal discomfort to patients, and provide information about normal or elevated ICP levels to the physicians.