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Active, not recruiting Not applicable Interventional

Post Approval Study - Evaluate the Long-Term Safety and Effectiveness of the WEB Device

ClinicalTrials.gov ID: NCT04839705

Public ClinicalTrials.gov record NCT04839705. Field values are reproduced from the official study page; the official ClinicalTrials.gov record remains the source of truth for eligibility, enrollment, and contact information.

ClinicalTrials.gov public records Last synced May 20, 2026, 6:21 AM EDT

Data is sourced from official ClinicalTrials.gov public API records. Always review the official ClinicalTrials.gov record for the latest information.

Official title

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

Study identification

NCT ID
NCT04839705
Recruitment status
Active, not recruiting
Study type
Interventional
Phase
Not applicable
Lead sponsor
Microvention-Terumo, Inc.
Industry
Enrollment
195 participants

Conditions and interventions

Interventions

  • WEB Device

Device

Eligibility (public fields only)

Age range
18 Years and older
Sex
All
Healthy volunteers
Healthy volunteers not accepted

This page does not interpret eligibility. Detailed inclusion and exclusion criteria are on the official ClinicalTrials.gov record.

Study timeline

Start date
Aug 23, 2022
Primary completion
Apr 30, 2026
Completion
Apr 30, 2030
Last update posted
Mar 26, 2026

2022 – 2030

United States locations

U.S. sites
27
U.S. states
16
U.S. cities
24
Facility City State ZIP Site status
Memorial Health Systems Hollywood Florida 33021
Orlando Health Neuroscience Institute Orlando Florida 32806
The Queen's Medical Center Neuroscience Institute Honolulu Hawaii 96813
University of Iowa Hospitals and Clinics Iowa City Iowa 52242
University of Kansas Health System Kansas City Kansas 66160
Baptist Health Systems Lexington Kentucky 40503
University of Kentucky, Department of Neurosurgery Lexington Kentucky 40536
Norton Healthcare Louisville Kentucky 40241
LSU Health Sciences Center at Shreveport Shreveport Louisiana 71103
Johns Hopkins University Baltimore Maryland 21287
Massachusetts General Brigham Incorporated Boston Massachusetts 02114
UMass Memorial Health Worcester Massachusetts 01655
Abbott Northwestern Hospital Allina Health Minneapolis Minnesota 55407
The Washington University St Louis Missouri 63110
Albany Medical Center Albany New York 12208
University of Buffalo Buffalo New York 14203
Northshore University Hospital/Northwell Health Manhasset New York 11030
SUNY Stony Brook Stony Brook New York 11794
Montefiore Medical Center The Bronx New York 10467
Ohio State University Columbus Ohio 43210
OhioHealth Research Institute Columbus Ohio 43214
The Toledo Hospital d/b/a ProMedica Toledo Hospital Toledo Ohio 43606
University of Oklahoma Health Sciences Center Oklahoma City Oklahoma 73104
University of Pennsylvania Health Systems Philadelphia Pennsylvania 19104
Thomas Jefferson University Hospital Philadelphia Pennsylvania 19107
Semmes Murphey Memphis Tennessee 38120
West Virginia University Morgantown West Virginia 26506

Site contact phone numbers, emails, and investigator names are intentionally not displayed here. Open the official ClinicalTrials.gov record for site contact information.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT04839705, including study identification, conditions, interventions, eligibility (age, sex, healthy volunteer), timeline, and U.S. site list.
What this page does not do
No medical advice, eligibility judgments, treatment recommendations, study quality scoring, or AI-generated medical summaries. No site contact phone numbers, emails, or investigator names.
Where the data comes from
Sourced from the official ClinicalTrials.gov public API. The official record is the source of truth.
Last refresh
Last update posted Mar 26, 2026 · Synced May 20, 2026

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Open the official record

The complete protocol, eligibility criteria, and contact information for NCT04839705 live on ClinicalTrials.gov.

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