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NCT06501872 · ClinicalTrials.gov registry record · NA

Safety and Effectiveness of Physician-Modified Fenestrated and Branched Aortic Endografting for the Treatment of Thoracoabdominal and Pararenal Aortic Aneurysms

A NA study of Aortic Aneurysm, sponsored by Bjoern D. Suckow.

Recruiting
Registry status
NA
Development phase
80
Enrollment target
1
Study location

NCT06501872 is a NA study of Aortic Aneurysm that is actively recruiting participants, run by Bjoern D. Suckow. The registered enrollment target is 80 participants, below the 634-participant average among 14 other Aortic Aneurysm trials with a reported enrollment target (87% lower). The trial reports 1 study location across 1 state.

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The verdict

NCT06501872, a NA study of Aortic Aneurysm, is actively recruiting participants, sponsored by Bjoern D. Suckow.

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

Study Summary

The primary clinical objective of this study is to evaluate the safety and effectiveness of a physician-modified, fenestrated and branched aortic endoprosthesis for the treatment of thoracoabdominal aortic aneurysms (TAAAs). The goal of the primary analysis is to demonstrate both the safety and effectiveness of using a physician-modified fenestrated Cook Zenith Alpha Thoracic Endovascular Graft as compared to previously published results of open surgical replacement of the aneurysmal aorta.

Conditions Studied

Interventions

  • DEVICE Physician-modified aortic endograft

Study Locations (1)

New Hampshire

  • Dartmouth-Hitchcock Medical Center - Lebanon

Trial Details

FieldValue
Enrollment Target 80 participants
Start Date 2024-12-10
Est. Completion 2031-09
Phase NA

Sponsor

Bjoern D. Suckow

1 total trials

What the Registry Record Tells You About NCT06501872

The ClinicalTrials.gov registry entry for NCT06501872 describes a study currently listed as recruiting, categorized as NA. The registered enrollment target is 80 participants, a figure that helps gauge the scale of data the investigators plan to collect, below the 634-participant average among 14 other Aortic Aneurysm trials with a reported enrollment target (87% lower). The listed sponsor is Bjoern D. Suckow, which has 1 total studies on file at ClinicalTrials.gov.

The record links to 1 condition, with Aortic Aneurysm appearing as the primary indexed condition, and to 1 intervention - of which Physician-modified aortic endograft is the first listed.

NCT06501872 reports 1 study location spanning 1 distinct geographic area - top geographies include New Hampshire.

Frequently Asked Questions

What is clinical trial NCT06501872 about?

NCT06501872 is a clinical study titled "Safety and Effectiveness of Physician-Modified Fenestrated and Branched Aortic Endografting for the Treatment of Thoracoabdominal and Pararenal Aortic Aneurysms". The primary clinical objective of this study is to evaluate the safety and effectiveness of a physician-modified, fenestrated and branched aortic endoprosthesis for the treatment of thoracoabdominal aortic aneurysms (TAAAs). The goal of the primary analysis is to demonstrate both the safety and effe...

What is the current status of trial NCT06501872?

This trial is currently recruiting. It is a NA study. The enrollment target is 80 participants. The study started on 2024-12-10. Estimated completion is 2031-09.

What conditions does trial NCT06501872 study?

This clinical trial studies the following conditions: Aortic Aneurysm.

What interventions are being tested in trial NCT06501872?

The interventions under investigation include: Physician-modified aortic endograft (DEVICE).

Who is sponsoring clinical trial NCT06501872?

This trial is sponsored by Bjoern D. Suckow, which has 1 total clinical trials registered on ClinicalTrials.gov.

Where is trial NCT06501872 being conducted?

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

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