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NCT05501002

Pilot Study to Evaluate the CereVasc® EShunt® System in the Treatment of Communicating Hydrocephalus

Terminated NA Last updated 22 November 2024
What this trial tests

NA trial testing eShunt® Implant in Hydrocephalus in 4 participants. Terminated before completion.

Timeline
15 September 2022
Primary endpoint
15 September 2023
15 September 2023

Quick facts

Lead sponsorCereVasc Inc
PhaseNA
StatusTerminated
Study typeINTERVENTIONAL
Allocationna
Designsingle group
Maskingnone
Primary purposetreatment
Enrollment4
Start date15 September 2022
Primary completion15 September 2023
Estimated completion15 September 2023
Sites2 locations across United States

Drugs / interventions tested

Conditions studied

Sponsor

CereVasc Inc — full company profile →

Who can join

21 and older, any sex, with Hydrocephalus or Hydrocephalus, Communicating. Patients with the condition only — healthy volunteers not accepted.

Sponsor's own description

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.

Publications & conference data

1 peer-reviewed publication reference this trial (live from Europe PMC):

  1. A minimally invasive endovascular approach to the cerebellopontine angle cistern enables broad CNS biodistribution of scAAV9-CB-GFP.
    Benatti HR, Anagnostakou V, Taghian T, Hall EF, et al · · 2024 · cited 4× · PMID 39192584 · DOI 10.1016/j.ymthe.2024.08.024

Verify or expand the search:

Other recruiting trials for Hydrocephalus

Currently open trials in the same condition.

Other CereVasc Inc trials

Trials by the same sponsor.

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Data sources for this page

Drug Landscape aggregates and links these public records for informational use only. Always verify against the primary source before clinical or regulatory decisions. Canonical URL: https://druglandscape.com/trial/NCT05501002.

Primary sources · FDA · ClinicalTrials.gov · EMA · SEC EDGAR · ChEMBL · Wikidata · full sourcing