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NCT06308094 · ClinicalTrials.gov registry record · NA

320-detector Computed Tomography to Assess Myocardial Extracellular Volume Fraction in Patients With Atrial Fibrillation Before AF Ablation.

A NA study of Atrial Fibrillation, sponsored by Johns Hopkins University.

Recruiting
Registry status
NA
Development phase
100
Enrollment target
1
Study location

NCT06308094: Recruiting NA study of Atrial Fibrillation, sponsored by Johns Hopkins University.

NCT06308094 is a NA study of Atrial Fibrillation that is actively recruiting participants, run by Johns Hopkins University. The registered enrollment target is 100 participants, below the 2,996-participant average among 202 other Atrial Fibrillation trials with a reported enrollment target (97% 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

NCT06308094, a NA study of Atrial Fibrillation, is actively recruiting participants, sponsored by Johns Hopkins University.

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

Study Summary

This study explores the relationship between myocardial fibrosis and patient outcomes in Atrial Fibrillation (AF), specifically after catheter ablation. It aims to use Cardiac CT, an accessible tool, to measure left ventricular extracellular volume (ECV) as an indicator of fibrosis. The study will assess if higher ECV levels correlate with increased risks of AF recurrence, hospitalization, and poor cardiac function recovery. Positive findings could make ECV a key factor in deciding AF treatment strategies.

Primary Outcome

Patients will undergo computed tomography (CT) imaging with a total of 4 CT image acquisition (2 clinical and 2 research) During the follow-up visit with the primary electrophysiologist within 90 days after the procedure, the patient will be assessed for recurrence of atrial fibrillation.

Conditions Studied

Interventions

  • DIAGNOSTIC_TEST CT

Study Locations (1)

Maryland

  • Johns Hopkins Hospital - Baltimore

Trial Details

FieldValue
Enrollment Target 100 participants
Start Date 2025-04-10
Est. Completion 2026-04-01
Phase NA
Johns Hopkins University

1,448 total trials

What NCT06308094 shows while recruiting

NCT06308094 is an interventional study that assigns participants to a tested intervention. The registered 100 participants enrollment target is mid-sized for trials with a published cap, below the 2,996-participant average among 202 other Atrial Fibrillation trials with a reported enrollment target (97% lower).

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

NCT06308094 reports a single indexed study location in Maryland.

Frequently Asked Questions

What is clinical trial NCT06308094 about?

NCT06308094 is a clinical study titled "320-detector Computed Tomography to Assess Myocardial Extracellular Volume Fraction in Patients With Atrial Fibrillation Before AF Ablation.". This study explores the relationship between myocardial fibrosis and patient outcomes in Atrial Fibrillation (AF), specifically after catheter ablation. It aims to use Cardiac CT, an accessible tool, to measure left ventricular extracellular volume (ECV) as an indicator of fibrosis. The study will a...

What is the current status of trial NCT06308094?

This trial is currently recruiting. It is a NA study. The enrollment target is 100 participants. The study started on 2025-04-10. Estimated completion is 2026-04-01.

What conditions does trial NCT06308094 study?

This clinical trial studies the following conditions: Atrial Fibrillation.

What interventions are being tested in trial NCT06308094?

The interventions under investigation include: CT (DIAGNOSTIC_TEST).

Who is sponsoring clinical trial NCT06308094?

This trial is sponsored by Johns Hopkins University, which has 1,448 total clinical trials registered on ClinicalTrials.gov.

Where is trial NCT06308094 being conducted?

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

Similar trials for Atrial Fibrillation

Matched on the same primary condition, ranked to surface studies in the same phase first, then by recruiting status, no relevance scoring or editorial curation.

Where NCT06308094's enrollment target sits among peer trials

100 139th of 202 higher than 59 of 202 other Atrial Fibrillation trials

participants (enrollment target), bucketed by value

Each bar is a band; taller bars hold more other Atrial Fibrillation 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 NCT06308094, the US trial registry maintained by the National Library of Medicine. NCT06308094 (mid enrollment · single site footprint · recruiting) retrieved and formatted by PlainTrial, see methodology.