US Pilot Study to Evaluate the Safety and Effectiveness of the CereVasc® EShunt® System in the Treatment of Communicating Hydrocephalus
Overview
- Phase
- Not Applicable
- Intervention
- Not specified
- Conditions
- Hydrocephalus
- Sponsor
- CereVasc Inc
- Enrollment
- 4
- Locations
- 2
- Primary Endpoint
- Reduction in ICP
- Status
- Terminated
- Last Updated
- last year
Overview
Brief Summary
The purpose of this study will be to evaluate a novel, minimally invasive method of treating hydrocephalus in adults. The eShunt® System includes a proprietary eShunt® Delivery System and the eShunt® Implant, a permanent implant that is deployed in a mildly invasive, neuro-interventional procedure. The eShunt® Implant is designed to drain excess cerebrospinal fluid (CSF) from the intracranial subarachnoid space (SAS) into the venous system.
Detailed Description
This is a prospective, multi-center, open label, pilot study of the eShunt® System. The study population consists of patients with post-aneurysmal subarachnoid hemorrhage (SAH) treated for increased intracranial pressure (ICP) resulting in symptomatic hydrocephalus using an external ventricular drain (EVD) to facilitate CSF drainage and who cannot be "weaned" from the EVD after the hemorrhagic event. After completion of the procedure to place the eShunt® device, the ICP will be monitored and recorded for up to 48 hours. Subjects will then return for follow-up visits that include standard neurological evaluations at 30, 60, 90, 180, and 365 days postimplantation; imaging will also be acquired at 30, 90 and 365 days after implant. Subjects will continue to attend follow-up visits every 180 days thereafter until the study is closed or up to 5 years post-implantation.
Investigators
Eligibility Criteria
Inclusion Criteria
- •Patient is ≥ 21 years old
- •Patient or legally authorized representative is able and willing to provide written informed consent
- •Post-aneurysmal SAH with Hunt and Hess Grades I-IV with EVD in place for at least 7 days with the need for a permanent CSF shunt determined through a failed EVD clamping trial defined as:
- •Post-clamping ICP of \> 20 cmH2O for 15 minutes, or
- •Post-clamping ICP \> 25 cmH2O for \< 15 minutes with patient intolerance to EVD clamping, or
- •Significant radiographic signs of increasing ventriculomegaly, or
- •Neurological decline attributable to ventriculomegaly and requiring CSF diversion
- •Clinical signs and symptoms of communicating hydrocephalus
- •Neurologically stable without evidence of severe vasospasm
- •Pre-procedure MRI confirmation of anatomy suitable for eShunt Procedure, as described in Section 1.8.3.4.2 and confirmed by subject screening committee (SSC)
Exclusion Criteria
- •Presence of gross blood in CSF
- •Signs or symptoms of obstructive hydrocephalus
- •Active systemic infection or infection detected in CSF
- •Prior or existing shunts, endoscopic third ventriculostomy, or any previous surgical intervention for hydrocephalus
- •Hypersensitivity or contraindication to heparin or radiographic contrast agents which cannot be adequately pre-medicated, desensitized or where no alternative is available
- •Occlusion or stenosis of the internal jugular vein
- •Venous distension in the neck on physical exam
- •Medical conditions associated with prolonged elevation of jugular venous pressure, including jugular vein stenosis or stricture, right sided heart failure, cirrhosis of the liver, arterial venous fistulas in the arm for dialysis purposes, or an arterial venous fistula or malformation in the neck or brain
- •Atrial septal defect or patent foramen ovale identified on cardiac echocardiogram
- •History of bleeding diatheses, coagulopathy or will refuse blood transfusion in cases of emergency
Outcomes
Primary Outcomes
Reduction in ICP
Time Frame: 24-48 hours after eShunt Implant placement
At 24 to 48 hours after eShunt Implant deployment (with EVD remaining clamped) an ICP measurement that indicates: * ICP below 20 cmH2O with no periods longer than 15 minutes above 20 cmH2O * No episodes of ICP above 25 cmH2O with associated symptoms
Secondary Outcomes
- Incidence of clinically significant changes in Computed Tomography Imaging (CT/CTA) from baseline.(1 year post procedure)
- Changes in Modified Rankin Scale Scores(1 year post procedure)
- Summary of Adverse Events(90 days post procedure and at study completion)
- Number of subjects requiring conversion to conventional CSF shunt(1 year post procedure)
- Occurrence of Serious Adverse Events(90 days post procedure)
- Number of participants with clinically significant changes in physical and neurologic examination assessments from baseline(1 year post procedure)