Clinical Trials Directory

Trials / Terminated

TerminatedNCT02900222

Study of Choroid Plexus Cauterization in Patients With Hydrocephalus

Study of Endoscopic Choroid Plexus Cauterization for Adult Patients With Hydrocephalus and Risk Factors for Perioperative Complications Following Shunt Surgery.

Status
Terminated
Phase
N/A
Study type
Interventional
Enrollment
1 (actual)
Sponsor
Ronald Benveniste · Academic / Other
Sex
All
Age
18 Years
Healthy volunteers
Not accepted

Summary

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.

Conditions

Interventions

TypeNameDescription
PROCEDUREendoscopic choroid plexus coagulationA burr hole will be made over the frontal lobe of the brain. An endoscope will be introduced into the ventricle of the brain and the choroid plexus coagulated with an electrocautery device. The septum pellucidum separating the right and left lateral ventricles will be opened, and the choroid plexus on the opposite side coagulated as well.

Timeline

Start date
2016-09-01
Primary completion
2018-05-16
Completion
2018-05-16
First posted
2016-09-14
Last updated
2021-06-11

Locations

1 site across 1 country: United States

Source: ClinicalTrials.gov record NCT02900222. Inclusion in this directory is not an endorsement.