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Third Ventriculostomy Versus Shunt for Children With Hydrocephalus

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Duke University

Status

Completed

Conditions

Communicating Hydrocephalus

Treatments

Procedure: Ventricular shunt
Procedure: Endoscopic third ventriculostomy (ETV)

Study type

Interventional

Funder types

Other

Identifiers

NCT01801267
Pro00043098

Details and patient eligibility

About

Ventriculoperitoneal shunts are the standard of care for patients with communicating hydrocephalus, but they have a high failure rate - up to 40% fail within 1 year and 50% fail within 2 years. It has long been assumed that endoscopic third ventriculostomy (ETV) would not work in this population and is better suited to patients with obstructive hydrocephalus (such as from a tumor blocking cerebral-spinal fluid (CSF) pathways). However, as scientists learn more about CSF and the way our brains absorb this fluid, they have learned that this may not be so straight-forward. Recent small studies have shown that ETVs can work in a good percentage of children with communicating hydrocephalus, too. But no randomized controlled trials have been done to compare these two treatments directly to determine which will provide children with a better prognosis, fewer surgeries over their lifetime, less time in the hospital and the greatest chance at as normal a life as possible.

The investigators will conduct a trial to compare these two surgical treatments where patients will be randomized to receive either a shunt or an ETV. Because ETV has been shown to have a high failure rate in newborns, the investigators will not include these patients and instead will study patients who come to Duke University with communicating hydrocephalus between the ages of 1 year and 18 years. The study will include patients with ventricular shunts who are in need of revision and patients who were just diagnosed and need their first shunt.

All patients who agree to participate will be randomized to receive either an ETV or a shunt. The study team will follow them for one year from the time of the surgery and will determine what percentage of patients require further CSF-related surgeries, how long they go after their surgery before they need another surgery, how much time they spend in the hospital and what percentage of patients suffer CSF-infections or other problems related to the surgery or their hydrocephalus. The study team will examine these results and determine if ETV is a safer or more effective treatment for children with communicating hydrocephalus than is a ventricular shunt.

Enrollment

8 patients

Sex

All

Ages

1 to 18 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Children age 1-18 years
  • Patients with communicating hydrocephalus who present in need of CSF diversion surgery, as diagnosed by radiographic imaging (CT or MRI of brain) as well as clinical signs or symptoms of increased intracranial pressure
  • Informed consent according to institutional guidelines must be obtained from each patient's parent or legal guardian, or by the patient him/herself if he/she is 18 years of age

Exclusion criteria

  • An active Central Nervous System malignancy (cancer)
  • The presence of two or more current ventricular catheters indicating that the ventricles do not communicate with each other
  • The inability of the parent/guardian or patient to provide informed consent

Trial design

Primary purpose

Treatment

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

None (Open label)

8 participants in 2 patient groups

Endoscopic third ventriculostomy (ETV)
Experimental group
Description:
Pediatric patients in need of CSF-diversion surgery will undergo an endoscopic third ventriculostomy (ETV).
Treatment:
Procedure: Endoscopic third ventriculostomy (ETV)
Ventricular shunt
Active Comparator group
Description:
Pediatric patients in need of CSF-diversion surgery will undergo ventricular shunt placement or revision.
Treatment:
Procedure: Ventricular shunt

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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