Back

POST-MARKET SURVEILLANCE STUDY TO EVALUATE THE LONG-TERM SAFETY AND EFFECTIVENESS OF THE WEB® DEVICE

Post-Approval Study – Post-Market Surveillance Study to Evaluate the Long-Term Safety and Effectiveness of the WEB Device

  • Clinical Trial Information

    Trial Contact: Carlo, Charlene S; Monserrate, Francheska; Flores-Vega, Mariangelis; Melendez, Thomas L

  • IRB No: W22.173.08

    Protocol Abbrev: WEB_PAS

    Principal Investigator: Jay Ashok Vachhani, MD

    Phase: Device: Significant Risk

    Age Group: Adult

    Secondary Protocol No: CL11010-001

    Treatment: WEB Device

    Therapies Involved: Surgery

    ClinicalTrials.gov ID: NCT04839705

  • Objective

    Post-market study to evaluate the long-term safety and effectiveness of the WEB Device within currently approved indications for use.

  • Key Eligibility

    Adult subjects with intracranial wide-neck aneurysms located at arterial bifurcations.