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
| Type | Name | Description |
|---|---|---|
| PROCEDURE | endoscopic choroid plexus coagulation | A 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.