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NCT06793059 · ClinicalTrials.gov registry record · NA

Evaluation of Flow Diverter Technology Device for Intracranial Aneurysm (SHIELD)

A NA study of Aneurysm, sponsored by Jacobs institute.

Recruiting
Registry status
NA
Development phase
10
Enrollment target
1
Study location

NCT06793059: Recruiting NA study of Aneurysm, sponsored by Jacobs institute.

NCT06793059 is a NA study of Aneurysm that is actively recruiting participants, run by Jacobs institute. The registered enrollment target is 10 participants, below the 17,095-participant average among 6 other Aneurysm trials with a reported enrollment target (100% lower). The trial reports 1 study location across 1 state. According to ClinicalTrials.gov, the official US trial registry.

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The verdict

NCT06793059, a NA study of Aneurysm, is actively recruiting participants, sponsored by Jacobs institute.

RECRUITING
Registry status
NA
Development phase
10 participants
Enrollment target
1
Study location

Study Summary

The Jacobs Institute is participating in a study designed to collect prospective clinical evidence to evaluate the approved use of the Pipeline™ Flex Embolization Device with Shield Technology™ for the endovascular treatment of adults (22 years of age or older) with wide-necked intracranial aneurysms

Primary Outcome

The Pipeline™ Flex Embolization Device with Shield Technology™ for the endovascular treatment of adults (22 years of age or older) with large or giant wide-necked intracranial aneurysms (IAs) in the internal carotid artery from the petrous to the superior hypophyseal segments. The Pipeline™ Flex Embolization Device with Shield Technology™ is also indicated for use in the internal carotid artery up to the terminus for the endovascular treatment of adults (22 years of age or older) with small and

Conditions Studied

Interventions

  • DEVICE SHIELD

Study Locations (1)

New York

  • Jacobs Institute - Buffalo

Trial Details

FieldValue
Enrollment Target 10 participants
Start Date 2025-01-01
Est. Completion 2027-01-01
Phase NA
Jacobs institute

5 total trials

What NCT06793059 shows while recruiting

NCT06793059 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 10 participants, a relatively small participant target, below the 17,095-participant average among 6 other Aneurysm trials with a reported enrollment target (100% lower).

The record links to 1 condition, with Aneurysm appearing as the primary indexed condition, and to 1 intervention - of which SHIELD is the first listed.

NCT06793059 reports a single indexed study location in New York.

Frequently Asked Questions

What is clinical trial NCT06793059 about?

NCT06793059 is a clinical study titled "Evaluation of Flow Diverter Technology Device for Intracranial Aneurysm (SHIELD)". The Jacobs Institute is participating in a study designed to collect prospective clinical evidence to evaluate the approved use of the Pipeline™ Flex Embolization Device with Shield Technology™ for the endovascular treatment of adults (22 years of age or older) with wide-necked intracranial aneurysm...

What is the current status of trial NCT06793059?

This trial is currently recruiting. It is a NA study. The enrollment target is 10 participants. The study started on 2025-01-01. Estimated completion is 2027-01-01.

What conditions does trial NCT06793059 study?

This clinical trial studies the following conditions: Aneurysm.

What interventions are being tested in trial NCT06793059?

The interventions under investigation include: SHIELD (DEVICE).

Who is sponsoring clinical trial NCT06793059?

This trial is sponsored by Jacobs institute, which has 5 total clinical trials registered on ClinicalTrials.gov.

Where is trial NCT06793059 being conducted?

This trial has 1 study location across New York. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.

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Source: ClinicalTrials.gov NCT06793059, the US trial registry maintained by the National Library of Medicine. NCT06793059 (small enrollment · single site footprint · recruiting) retrieved and formatted by PlainTrial, see methodology.