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NCT03946072 · ClinicalTrials.gov registry record · NA

Transseptal vs Retrograde Aortic Ventricular Entry to Reduce Systemic Emboli

A NA study, sponsored by University of California, San Francisco.

Completed
Registry status
NA
Development phase
153
Enrollment target

NCT03946072: Completed NA study, sponsored by University of California, San Francisco.

NCT03946072 is a NA study that has completed, run by University of California, San Francisco. The registered enrollment target is 153 participants, below the 1,404-participant average among 58,714 other NA trials with a reported enrollment target (89% lower). According to ClinicalTrials.gov, the official US trial registry.

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The verdict

NCT03946072, a NA study, has completed, sponsored by University of California, San Francisco.

COMPLETED
Registry status
NA
Development phase
153 participants
Enrollment target

Study Summary

This study is a prospective, multicenter, randomized (1:1) controlled comparative effectiveness trial of a transseptal approach to left ventricular ablation compared to a retrograde aortic approach to prevent cerebral emboli and neurocognitive decline in adults with ventricular tachycardia (VT) and/or premature ventricular contractions (PVCs).

Primary Outcome

incidence of new cerebral embolic lesions measured by magnetic resonance imaging (MRI) post-ablation as compared to pre-ablation imaging studies

Interventions

  • PROCEDURE Transseptal Aortic Approach Catheter Ablation Procedure
  • PROCEDURE Retrograde Aortic Approach Catheter Ablation Procedure

Trial Details

FieldValue
Enrollment Target 153 participants
Start Date 2019-07-02
Est. Completion 2023-11-25
Phase NA

What the finished NCT03946072 record still lists

NCT03946072 is an interventional study that assigns participants to a tested intervention. The registered 153 participants enrollment target is mid-sized for trials with a published cap, below the 1,404-participant average among 58,714 other NA trials with a reported enrollment target (89% lower).

The record links to 0 conditions, and to 2 interventions - of which Transseptal Aortic Approach Catheter Ablation Procedure is the first listed.

NCT03946072 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT03946072 about?

NCT03946072 is a clinical study titled "Transseptal vs Retrograde Aortic Ventricular Entry to Reduce Systemic Emboli". This study is a prospective, multicenter, randomized (1:1) controlled comparative effectiveness trial of a transseptal approach to left ventricular ablation compared to a retrograde aortic approach to prevent cerebral emboli and neurocognitive decline in adults with ventricular tachycardia (VT) and/...

What is the current status of trial NCT03946072?

This trial is currently completed. It is a NA study. The enrollment target is 153 participants. The study started on 2019-07-02. Estimated completion is 2023-11-25.

What interventions are being tested in trial NCT03946072?

The interventions under investigation include: Transseptal Aortic Approach Catheter Ablation Procedure (PROCEDURE), Retrograde Aortic Approach Catheter Ablation Procedure (PROCEDURE).

Who is sponsoring clinical trial NCT03946072?

This trial is sponsored by University of California, San Francisco, which has 1,713 total clinical trials registered on ClinicalTrials.gov.

How this trial's enrollment target compares

Where NCT03946072's enrollment target sits among peer trials

153 656th of 2000 higher than 1,343 of 2,000 other NA trials

participants (enrollment target), bucketed by value

Each bar is a band; taller bars hold more other NA trials. The dashed line + filled bar mark this entry. Hover or tap any bar for its full count and share, and where it sits relative to this entry.

Source ClinicalTrials.gov registry export · 2026-08-08

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Source: ClinicalTrials.gov NCT03946072, the US trial registry maintained by the National Library of Medicine. NCT03946072 (mid enrollment · none site footprint · completed) retrieved and formatted by PlainTrial, see methodology.