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A Study Comparing Two Treatments for Infants With Hydrocephalus

International Infant Hydrocephalus Study: A Multicentre, Prospective Study

Status
Completed
Phases
Phase 2
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT00652470
Enrollment
182
Registered
2008-04-03
Start date
2005-09-30
Completion date
2018-05-01
Last updated
2018-09-10

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Hydrocephalus

Keywords

infants, Hydrocephalus, Cerebrospinal Fluid Shunt, Ventriculostomy, neurosurgery

Brief summary

The purpose of this study is to study whether infants with triventricular hydrocephalus (TVH) have a better long-term outcome at 5 years when they are treated with a new procedure, endoscopic third ventriculostomy (ETV), than infants treated with the more traditional treatment, insertion of a cerebrospinal fluid (CSF) shunt.

Detailed description

TVH is a relatively uncommon condition in infants, in which CSF accumulates in the brain's ventricles due to a blockage in outflow at the level of cerebral aqueduct. This can cause increased intracranial pressure, with adverse effect on brain development. The causes of this include congenital aqueductal stensois or acquired aqueductal stenosis from previous brain hemorrhage or infection. TVH is currently treated through one of the following two approaches: * Extra-cranial CSF diversion through ventricular shunts. Extra-cranial shunting has been the standard approach over the past few decades, since functional shunts were first developed and inserted successfully. * Intra-cranial internal CSF diversion using endoscopic techniques. The principles of internal diversion were clear from the time neurosurgeons first understood the nature of hydrocephalus. However, internal diversion was never really practical or successful on a large scale until the more recent development of neuroendoscopy. There is currently a revived interest in diversionary hydrocephalus treatment through neuroendoscopic surgical techniques, with the primary focus on endoscopic third ventriculostomy (ETV).

Interventions

A standard frontal burr hole will be made and an endoscopic camera used to visualize the floor of the third ventricle. A ventriculostomy will be created in the floor of the third using the surgeon's own preferred method of perforation.

PROCEDURECSF Shunt Insertion

The procedure involves creating a burr hole in the frontal or occipital regions and cannulating the ventricle with a silastic catheter. This is then attached to a valve mechanism and distal silastic tubing which runs subcutaneously in the peritoneal cavity.

Sponsors

The International Study Group for Neuroendoscopy (ISGNE)
CollaboratorUNKNOWN
The International Society for Pediatric Neurosurgery
CollaboratorOTHER
The Hospital for Sick Children
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
1 Days to 24 Months
Healthy volunteers
No

Inclusion criteria

* Symptomatic TVH requiring treatment. * No previous treatment for TVH * Under 24 months of age at time of surgery * Full-term pregnancy (\>36 weeks) * Mandatory pre-operative MRI that includes mid-sagittal T1 & T2 scans which show: Tri-ventricular pattern of hydrocephalus; proof of no flow through aqueduct; presence of CSF collection over the convexity and/or inter-hemispheric fissure is acceptable; configuration of third ventricle floor could vary; deformed tectal plate is acceptable; posterior fossa fluid collections may be included as long as: aqueduct is closed; vermis preserved (complete Dandy Walker Syndrome excluded); questionable flow in aqueduct acceptable as long as TVH exists * History or suggestion of intra-ventricular bleed (intra-uterine or post-natal) or intracranial infection qualifies (excluding intraventricular hemorrhage of prematurity). * Ability to participate in followup for at least 5 years

Exclusion criteria

* Open Spina Bifida * Complete Dandy Walker syndrome (vermian agenesis / dysgenesis) * Prematurity * Perinatal asphyxia * Severe dysmorphic anatomical features or known chromos (e.g. agenesis of corpus callosum, heterotopias, large cysts) * intracranial tumor

Design outcomes

Primary

MeasureTime frame
Health Status Outcome as measured by the Health Utilities Index - 2At 5 years of age

Secondary

MeasureTime frame
Neurodevelopment as measured by the Denver Developmental Screening TestUp to 3 years of Age
Health status outcome using the Hydrocephalus Outcome QuestionnaireAt 5 years of Age
In-depth Evaluation of Neurodevelopment, Functioning and Intelligence, as mesured by the Weschler Intelligence Scale for Children or Weschler Preschool and Primary Scale of IntelligenceAt 5 years of Age
Number of Subsequent Hydrocephalus-Related OperationsDuration of the Study
Surgical MorbidityDuration of the Study
DeathDuration of the Study
Hospitalization Time5 years post-operation
Need for repeat radiological scansDuration of the Study
Complications such as CNS infection, focal neurological deficit, significant hemorrhage, seizures requiring medicationDuration of the Study
Ventricular size and the existence of flow void (ETV group)assessed through radiological evaluation3 years of age
Incidence of failure of initial interventionDuration of the Study

Countries

Argentina, Brazil, Canada, Germany, Hungary, India, Israel, Italy, Netherlands, Poland, Russia, Serbia, Spain, Turkey (Türkiye), United Kingdom, United States

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Mar 13, 2026