Medical Information Only. Always consult your healthcare provider before enrolling in any clinical trial.

NCT07647939 · ClinicalTrials.gov registry record · NA

Exclusion of Left Atrial Appendage Thrombus in Emergency Department Patients With Atrial Fibrillation Undergoing CT to Assess for Pulmonary Embolus: A Feasibility Study

A NA study, sponsored by Northwell Health.

Not yet
Registry status
NA
Development phase
60
Enrollment target

NCT07647939: Clinical Trial NA study, sponsored by Northwell Health.

NCT07647939 is a NA study that has not yet begun recruiting, run by Northwell Health. The registered enrollment target is 60 participants, below the 1,404-participant average among 58,714 other NA trials with a reported enrollment target (96% lower). According to ClinicalTrials.gov, the official US trial registry.

View on ClinicalTrials.gov ↗

View your shortlist →

The verdict

NCT07647939, a NA study, has not yet begun recruiting, sponsored by Northwell Health.

NOT YET RECRUITING
Registry status
NA
Development phase
60 participants
Enrollment target

Study Summary

This study aims to investigate whether a quick, additional CT scan of the heart, performed immediately after a standard CT scan for pulmonary embolism, can effectively detect blood clots in the left atrial appendage (LAA) in patients with atrial fibrillation. Detecting these clots is crucial before certain heart procedures to prevent stroke. Currently, a different, more involved procedure (Transesophageal Echocardiography - TEE) is often used. This study will assess if this additional CT scan is feasible, meaning if it can provide clear enough images to identify LAA clots without needing more contrast dye. The study will involve 60 patients, half receiving an "ungated" CT scan and the other half a "gated" CT scan (timed with their heart rhythm). The results of these scans will not be used for immediate patient care during the study, but rather to evaluate the CT scan technique itself. There is no direct benefit to participants, but the information gained could lead to faster diagnosis and reduced unnecessary testing for future patients.

Primary Outcome

The primary endpoint of this study is to test the hypothesis that less than or equal to 20% of the repeat CT scan (described above) will be indeterminate for the presence or absence of left atrial appendage thrombus. Additionally, the proportion of indeterminate gated CT scans will be compared to the proportion of indeterminate ungated CT scans.

Interventions

  • DEVICE Delayed Un-gated CT Scan for Left Atrial Appendage Thrombus
  • DEVICE Delayed Gated CT Scan for Left Atrial Appendage Thrombus

Trial Details

FieldValue
Enrollment Target 60 participants
Start Date 2026-07
Est. Completion 2027-06
Phase NA
Northwell Health

370 total trials

What is known before NCT07647939 opens enrollment

NCT07647939 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 60 participants, a relatively small participant target, below the 1,404-participant average among 58,714 other NA trials with a reported enrollment target (96% lower).

The record links to 0 conditions, and to 2 interventions - of which Delayed Un-gated CT Scan for Left Atrial Appendage Thrombus is the first listed.

NCT07647939 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT07647939 about?

NCT07647939 is a clinical study titled "Exclusion of Left Atrial Appendage Thrombus in Emergency Department Patients With Atrial Fibrillation Undergoing CT to Assess for Pulmonary Embolus: A Feasibility Study". This study aims to investigate whether a quick, additional CT scan of the heart, performed immediately after a standard CT scan for pulmonary embolism, can effectively detect blood clots in the left atrial appendage (LAA) in patients with atrial fibrillation. Detecting these clots is crucial before ...

What is the current status of trial NCT07647939?

This trial is currently not yet recruiting. It is a NA study. The enrollment target is 60 participants. The study started on 2026-07. Estimated completion is 2027-06.

What interventions are being tested in trial NCT07647939?

The interventions under investigation include: Delayed Un-gated CT Scan for Left Atrial Appendage Thrombus (DEVICE), Delayed Gated CT Scan for Left Atrial Appendage Thrombus (DEVICE).

Who is sponsoring clinical trial NCT07647939?

This trial is sponsored by Northwell Health, which has 370 total clinical trials registered on ClinicalTrials.gov.

How this trial's enrollment target compares

Where NCT07647939's enrollment target sits among peer trials

60 1164th of 2000 higher than 745 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

Nationwide trials with similar profiles

Cross-condition peers matched on enrollment target and registry start date, not the same-condition list above.

Similar enrollment target

  • NCT00576069 · 60 participants

    Mechanism(s)of Airflow Limitation in Moderate-severe Persistent Asthma

  • NCT01297400 · 60 participants · Phase 2

    Phase 2 Pilot Study of the Safety and Efficacy of Topical MW-III in Thermal Burns

  • NCT01734122 · 60 participants

    Stereotactic Radiosurgery for Essential Tremor and Parkinsonian Tremor

  • NCT01804634 · 60 participants · Phase 2

    Reduced Intensity Haploidentical BMT for High Risk Solid Tumors

Similar registry start date

  • NCT05988463 · started 2027-01-01 · Phase 1

    Dose-Escalation Study of Artesunate Patients With IPF

  • NCT07219706 · started 2026-12-10 · NA

    Dietary Fiber and Time Restricted Eating

  • NCT02831335 · started 2026-12-01

    Technical Development of Multi-Parametric Renocerebral MRI

  • NCT05962346 · started 2026-12 · NA

    Fetal Endoscopic Tracheal Occlusion for Congenital Diaphragmatic Hernia

Source: ClinicalTrials.gov NCT07647939, the US trial registry maintained by the National Library of Medicine. NCT07647939 (small enrollment · none site footprint · not yet recruiting) retrieved and formatted by PlainTrial, see methodology.