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NCT06693011 · ClinicalTrials.gov registry record · NA

Contour Neurovascular System™ ContiNued Access Investigational Device EXempTion (IDE) Trial (NEXT Trial)

A NA study of Cerebral Aneurysms, sponsored by Cerus Endovascular.

Recruiting
Registry status
NA
Development phase
250
Enrollment target
4
Study locations

NCT06693011 is a NA study of Cerebral Aneurysms that is actively recruiting participants, run by Cerus Endovascular. The registered enrollment target is 250 participants. The trial reports 4 study locations across 3 states.

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The verdict

NCT06693011, a NA study of Cerebral Aneurysms, is actively recruiting participants, sponsored by Cerus Endovascular.

RECRUITING
Registry status
NA
Development phase
250 participants
Enrollment target
4
Study locations

Study Summary

The goal of this clinical trial is to collect additional data to demonstrate if the Contour Neurovascular System (CNS) is a safe and effective treatment of wide-necked, saccular, intracranial aneurysms. Participants will: Undergo treatment with the Contour Neurovascular System Complete follow-up visits at 1month, 12months, and 24 months, following their procedure Report any adverse events to their study team

Conditions Studied

Interventions

  • DEVICE Contour Neurovascular System Treatment Attempt

Study Locations (4)

New York

  • University at Buffalo Neurosurgery - Buffalo
  • Stony Brook University - Stony Brook

Pennsylvania

  • University of Pennsylvania - Philadelphia

Washington

  • Swedish Neuroscience Institute - Seattle

Trial Details

FieldValue
Enrollment Target 250 participants
Start Date 2025-06-10
Est. Completion 2030-01
Phase NA

Sponsor

Cerus Endovascular

2 total trials

What the Registry Record Tells You About NCT06693011

The ClinicalTrials.gov registry entry for NCT06693011 describes a study currently listed as recruiting, categorized as NA. The registered enrollment target is 250 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is Cerus Endovascular, which has 2 total studies on file at ClinicalTrials.gov.

The record links to 1 condition, with Cerebral Aneurysms appearing as the primary indexed condition, and to 1 intervention - of which Contour Neurovascular System Treatment Attempt is the first listed.

NCT06693011 reports 4 study locations spanning 3 distinct geographic areas - top geographies include New York, Pennsylvania, Washington.

Frequently Asked Questions

What is clinical trial NCT06693011 about?

NCT06693011 is a clinical study titled "Contour Neurovascular System™ ContiNued Access Investigational Device EXempTion (IDE) Trial (NEXT Trial)". The goal of this clinical trial is to collect additional data to demonstrate if the Contour Neurovascular System (CNS) is a safe and effective treatment of wide-necked, saccular, intracranial aneurysms. Participants will: Undergo treatment with the Contour Neurovascular System Complete follow-up v...

What is the current status of trial NCT06693011?

This trial is currently recruiting. It is a NA study. The enrollment target is 250 participants. The study started on 2025-06-10. Estimated completion is 2030-01.

What conditions does trial NCT06693011 study?

This clinical trial studies the following conditions: Cerebral Aneurysms.

What interventions are being tested in trial NCT06693011?

The interventions under investigation include: Contour Neurovascular System Treatment Attempt (DEVICE).

Who is sponsoring clinical trial NCT06693011?

This trial is sponsored by Cerus Endovascular, which has 2 total clinical trials registered on ClinicalTrials.gov.

Where is trial NCT06693011 being conducted?

This trial has 4 study locations across New York, Pennsylvania, Washington. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.

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Data sourced from official public datasets. See our methodology for details. Retrieved and formatted by PlainTrial Editorial

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