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Hydrocephalus clinical trials

View clinical trials related to Hydrocephalus.

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NCT ID: NCT03350750 Completed - Clinical trials for Idiopathic Normal Pressure Hydrocephalus (INPH)

A Placebo-Controlled Effectiveness in INPH Shunting (PENS) Trial

PENS
Start date: May 21, 2018
Phase: N/A
Study type: Interventional

The Placebo-Controlled Effectiveness in Idiopathic Normal Pressure Hydrocephalus (iNPH) Shunting (PENS) trial is a multi-center blinded, randomized, placebo-controlled design investigation of cerebrospinal fluid (CSF) shunt surgery to study the shunt effectiveness in iNPH patients.

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: NCT02659111 Completed - Clinical trials for Hydrocephalus, Normal Pressure

Effects of Physical Training in iNPH

iNPhys
Start date: January 2016
Phase: N/A
Study type: Interventional

Patients with idiopathic Normal Pressure Hydrocephalus (iNPH) have variable difficulties regarding gait, balance, cognition and micturition. A shunt operation will improve these difficulties in most cases. Data suggest however, that they do not change their physical activity postoperatively. Physical training has been shown to be beneficial in patients with similar diseases i.e. Parkinson. The aim of this study is to apply a high intensity physical training program after a shunt operation to see if the patients can improve their physical capacity and ambulatory activity more than patients who only receive standardized written advice about physical training.

NCT ID: NCT02651337 Completed - Hydrocephaly Clinical Trials

Quantitative Characterization of Safe Irrigation for Ventricular Shunt Catheters

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

The objective of this pilot study is to perform a set of pressure and flow rate measurements in order to quantitatively characterize safe irrigation or "flushing" of a ventricular shunt catheter, a routine maneuver performed by a neurosurgeon during a shunt revision surgery. This maneuver involves injecting saline with a syringe to clear plugged shunt catheters. Based on data obtained in Stage I of the study, a device has been fabricated which provides the same small-volume pulse of fluid used by surgeons. In Stage II of the study, pressure and flow rate measurements generated by this specialized flusher device will be collected and measured.

NCT ID: NCT02575105 Completed - Hydrocephalus Clinical Trials

BIS Monitoring of Patients With Hydrocephalus

BIS1
Start date: May 2008
Phase:
Study type: Observational

We tested the hypothesis that BIS values are altered in pediatric patients with hydrocephaly. We also tested the hypothesis that BIS values are altered in adult post cerebral hemorrhage patients with hydrocephaly undergoing ventricular-peritoneal shunt placement

NCT ID: NCT02404740 Completed - Hydrocephalus Clinical Trials

Noninvasive Intracranial Pressure and Hydrocephalus Patients

Start date: February 2015
Phase:
Study type: Observational

Using a pulse oximeter, we have developed an algorithm that estimates intracranial pressure (ICP) based on patients who have had traumatic brain injuries. Patients with hydrocephalus are typically treated with a shunt in order to reduce ICP. At times the shunt can malfunction. We believe that our algorithm will help identify when a hydrocephalus patient's shunt has malfunctioned.

NCT ID: NCT02381977 Completed - Stroke Clinical Trials

Prevalence of Acute Critical Neurological Disease in Children: a Global Epidemiological Assessment

PANGEA
Start date: November 2011
Phase: N/A
Study type: Observational

PANGEA is an international prospective point prevalence study to describe the epidemiology, interventions, and outcomes in children with acute critical brain disease.

NCT ID: NCT02278848 Completed - Clinical trials for Chronic Adult Hydrocephalus

Multimodal Investigation in the Diagnosis and Treatment of Chronic Adult Hydrocephalus

Multimod'HCA
Start date: July 21, 2014
Phase: N/A
Study type: Interventional

Idiopathic chronic adult hydrocephalus (ICAH) is due to expansion of the fluid-filled cavities in the brain. The clinical symptoms are gait disturbance, mental decline and incontinence. Treatment involves installing a ventriculoperitoneal shunt which is known to be able to induce regression of the symptoms in many cases meaning that ICAH is a classic, curable cause of dementia. Diagnosis relies on comparing symptoms before and after depleting cerebrospinal fluid (CSF) via a lumbar puncture (LP). In practice, the situation is complicated: improvement is often incomplete and there is no consensus on either how to assess the symptoms or how they change after CSF depletion. In consequence, the decision whether not to undertake surgery often depends on the neurosurgeon's clinical impression. Over recent years, the cognitive profile of patients with ICAH has become better characterised and reproducible, objective techniques have been developed to assess motor function and CSF flow in the brain. The investigators project aims to define the value of these new investigative techniques in the positive diagnosis of ICAH, in comparison to current decision-making tools.

NCT ID: NCT02016352 Completed - Clinical trials for Normal Pressure Hydrocephalus

Cerebrospinal Fluid Proteome in Hydrocephalus

PROLIPHYC
Start date: March 2013
Phase: N/A
Study type: Interventional

PROLIPHYC is a collaborative prospective study that aims at discovering deep cerebrospinal fluid (CSF) proteome with a new clinically-compatible proteomics strategy, in a cohort of 100 patients suspected of neurodegenerative diseases and/or normal pressure hydrocephalus.