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NCT06584370 · ClinicalTrials.gov registry record · NA
Transatrial Pericardial Separation to Enhance Safety of Subxiphoid Pericardial Access for Left Atrial Appendage Ligation
A NA study of Atrial Fibrillation and Cardiac Catheterization, sponsored by Henry Ford Health System.
- Completed
- Registry status
- NA
- Development phase
- 13
- Enrollment target
- 1
- Study location
NCT06584370 is a NA study of Atrial Fibrillation and Cardiac Catheterization that has completed, run by Henry Ford Health System. The registered enrollment target is 13 participants, below the 2,997-participant average among 202 other Atrial Fibrillation trials with a reported enrollment target (100% lower). The trial reports 1 study location across 1 state.
The verdict
NCT06584370, a NA study of Atrial Fibrillation and Cardiac Catheterization, has completed, sponsored by Henry Ford Health System.
- COMPLETED
- Registry status
- NA
- Development phase
- 13 participants
- Enrollment target
- 1
- Study location
Study Summary
We use a tiny catheter through the heart to separate the pericardium with gas. We expect this to improve the safety of the Lariat procedure.
Conditions Studied
Interventions
- PROCEDURE Pericardial insufflation with carbon dioxide through a transatrial microcatheter
Study Locations (1)
Michigan
- Henry Ford Health System - Detroit
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 13 participants |
| Start Date | 2014-05 |
| Est. Completion | 2015-08 |
| Phase | NA |
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Full Details on ClinicalTrials.gov ↗What the Registry Record Tells You About NCT06584370
The ClinicalTrials.gov registry entry for NCT06584370 describes a study currently listed as completed, categorized as NA. The registered enrollment target is 13 participants, a figure that helps gauge the scale of data the investigators plan to collect, below the 2,997-participant average among 202 other Atrial Fibrillation trials with a reported enrollment target (100% lower). The listed sponsor is Henry Ford Health System, which has 234 total studies on file at ClinicalTrials.gov.
The record links to 9 conditions, with Atrial Fibrillation appearing as the primary indexed condition, and to 1 intervention - of which Pericardial insufflation with carbon dioxide through a transatrial microcatheter is the first listed.
NCT06584370 reports 1 study location spanning 1 distinct geographic area - top geographies include Michigan.
Frequently Asked Questions
What is clinical trial NCT06584370 about?
NCT06584370 is a clinical study titled "Transatrial Pericardial Separation to Enhance Safety of Subxiphoid Pericardial Access for Left Atrial Appendage Ligation". We use a tiny catheter through the heart to separate the pericardium with gas. We expect this to improve the safety of the Lariat procedure.
What is the current status of trial NCT06584370?
This trial is currently completed. It is a NA study. The enrollment target is 13 participants. The study started on 2014-05. Estimated completion is 2015-08.
What conditions does trial NCT06584370 study?
This clinical trial studies the following conditions: Atrial Fibrillation, Cardiac Catheterization, Cardiac Surgical Procedures, Left Atrial Appendage Ligation, Pericardium.
What interventions are being tested in trial NCT06584370?
The interventions under investigation include: Pericardial insufflation with carbon dioxide through a transatrial microcatheter (PROCEDURE).
Who is sponsoring clinical trial NCT06584370?
This trial is sponsored by Henry Ford Health System, which has 234 total clinical trials registered on ClinicalTrials.gov.
Where is trial NCT06584370 being conducted?
This trial has 1 study location across Michigan. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.
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