ClinicalTrials.gg
CompletedNCT07922655Updated Nov 6, 2026

From Skull Base to Atrial Fibrillation: Reduced Jugular Foramen Volume as a Structural Correlate of Atrial Fibrillation

An observational study in Atrial Fibrillation (AF), sponsored by Ankara Ataturk Sanatorium Training and Research Hospital. Completed at 1 site in Turkey (Türkiye). Open to participants aged 60 Years to 90 Years. Per ClinicalTrials.gov, last updated 2026-11-06.

Sponsored by Ankara Ataturk Sanatorium Training and Research Hospital · Observational

Updated Nov 6, 2026Newly registeredGo to Updates ↓
Study type
Observational
Model
Case-control
Time perspective
Cross-sectional
Enrollment
240
Ages
60 Years to 90 Years
Sex
All
01

Where this study stands

Counted across the records on this site · 2026-11-12

Among 55 studies in Atrial Fibrillation with a site in Turkey — 8 open to participants now, 9 under way, 2 of them phase 3. Atrial Fibrillation · Turkey.

Enrollment
16th of 25
240 · median 400
Started
2025
with 4 others
Observational
25 of 55
3 open now
Registered
55th of 55
by date
Lead sponsor
3 of 55
Ankara Ataturk Sanatorium Training and Research Hospital

Among the 55 studies in Atrial Fibrillation with a site in Turkey, this one is the 16th largest by enrollment of the 25 observational ones, is one of 5 that started in 2025, is one of 25 observational ones, and was the 55th registered.

By phase

55 studies; the count open now beside each. This study's row is marked.

Observationalthis study25 · 3 open
Phase 318 · 1 open
No phase10 · 3 open
Phase 42 · 1 open

By the year they started

First in 2003; this study’s year is marked. 5 started in 2025.

Size and results

Median enrollment 1,314 across the 30 interventional studies, 400 across the 25 observational. Of the 40 that completed or were terminated, 15 (38%) have results posted.

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Watch this landscapeDownload CSVWith an account: a weekly mail of what changed among 55 studies in Atrial Fibrillation with a site in Turkey, or all of them as a file.
02

Study summary

This study examines whether the size of the jugular foramen is associated with atrial fibrillation, a common irregular heart rhythm. The jugular foramen is an opening at the base of the skull through which nerves involved in heart regulation and a major vein pass.

This retrospective study uses existing medical records and head computed tomography (CT) scans from 240 adults aged 60-90 years: 120 with atrial fibrillation and 120 without a history of atrial fibrillation. Researchers measure the jugular foramina on both sides of the skull and compare their estimated volumes between the groups. They also examine whether any association remains after accounting for age, sex, skull size, other medical conditions, and heart ultrasound findings.

No additional scans, treatments, or patient visits are performed for this study. The study assesses an association and cannot establish whether jugular foramen size causes atrial fibrillation.

Read the detailed description

This single-center, retrospective case-control study evaluates jugular foramen morphology on archived cranial computed tomography (CT) images in relation to atrial fibrillation. The anatomical rationale is that the jugular foramen contains the vagus nerve and major venous structures. Differences in the dimensions of this bony opening may be associated with cardiac autonomic regulation, although the study does not directly measure nerve compression, venous pressure, or vagal function.

Participants are identified from an archive of non-contrast cranial CT examinations performed between January 2022 and July 2026. Cases have documented atrial fibrillation, while controls have no known history of atrial fibrillation and documented sinus rhythm. Selection is stratified by sex and three age bands: 60-69, 70-79, and 80-90 years. Each age-by-sex stratum includes 20 cases and 20 controls.

Two readers, blinded to atrial fibrillation status, independently assess thin-slice CT images using bone-window settings and multiplanar reconstructions. For each jugular foramen, the mediolateral diameter, anteroposterior diameter, and craniocaudal height are measured. Volume is estimated using an elliptical-cylinder model, and the right and left volumes are summed. Bony septation and cranial dimensions are also recorded. Measurements are averaged across readers for analysis. Interobserver and intraobserver agreement are assessed using intraclass correlation coefficients, and volume estimates are compared with semiautomatic segmentation in a subset of 40 participants.

Clinical characteristics and available laboratory measurements are extracted from existing records. Echocardiographic measures include the ratio of early mitral inflow velocity to early diastolic mitral annular velocity (E/e'), systolic pulmonary artery pressure, and left atrial volume index. Echocardiographic and rhythm documentation must be available within 12 months of the CT examination; laboratory measurements are obtained from records within three months of CT.

Analyses compare jugular foramen measurements between cases and controls overall and across age groups. Age-by-sex subgroup comparisons and interaction analyses are exploratory. Multivariable regression evaluates associations while accounting for demographic characteristics, cranial size, clinical factors, and echocardiographic findings. Receiver operating characteristic analyses assess the ability of jugular foramen volume and an age- and sex-adjusted volume score to distinguish cases from controls within the study sample.

All assessments use existing images and medical records. No study-specific imaging, treatment, or follow-up visits are performed. Because this is a retrospective case-control study, findings are interpreted as associations rather than evidence of causation. Any discrimination thresholds derived from this sample require independent validation.

03

Conditions studied

  • Atrial Fibrillation (AF)

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Keywords

  • Jugular foramen
  • Atrial fibrillation
  • Computed tomography
  • Skull base morphology
  • Jugular foramen volume
  • Vagus nerve
  • Retrospective case-control study
04

Who can participate

Ages eligible
60 Years to 90 Years
Sexes eligible
All
Accepts healthy volunteers
No
Sampling method
Non-probability sample

Study population

The study population consists of 240 adults aged 60-90 years selected from the cranial CT archive of a single hospital. Eligible CT examinations were performed between January 2022 and July 2026, with echocardiographic and cardiac rhythm documentation available within 12 months of CT. The sample includes 120 participants with documented atrial fibrillation and 120 controls with no history of atrial fibrillation and documented sinus rhythm. Participants were selected consecutively within age- and sex-defined strata, with 20 men and 20 women in each age band (60-69, 70-79, and 80-90 years) per group.

Go through the criteria one by one — yes, no or not sure — and take the list to your doctor or the study team. Kept in this browser only.

Inclusion criteria

Age 60-90 years.

Non-contrast cranial CT with bone reconstruction at a slice thickness of ≤0.625 mm, performed between January 2022 and July 2026.

Transthoracic echocardiography and cardiac rhythm documentation available within 12 months of the CT examination.

For the atrial fibrillation group: atrial fibrillation documented on a 12-lead or an ambulatory ECG recording lasting at least 30 seconds.

For the control group: no history of atrial fibrillation, sinus rhythm on all available electrocardiograms, and cranial CT performed for indications unrelated to the skull base.

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Exclusion criteria

Exclusion Criteria:

Atrial fibrillation attributable to transient reversible causes.

History of skull-base fracture, skull-base surgery, or skull-base tumor.

Fibrous dysplasia or Paget disease.

Jugular or sigmoid sinus thrombosis.

Intracranial hypertension.

More-than-moderate valvular heart disease.

Cardiomyopathy or congenital heart disease.

Prior cardiac surgery or catheter ablation.

Implanted devices.

CT image artifacts that prevent reliable jugular foramen measurements.

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Terms in these criteria, in plain language(1)

Underlined terms in the criteria open these too. Explained by clinicaltrials.gg, not part of the registry record. The study team decides who can take part.

ECG (electrocardiogram)

A recording of the heart’s electrical activity, taken with stickers on the chest, arms and legs. It takes a few minutes and does not hurt.

05

Study design

Observational model
Case-control
Time perspective
Cross-sectional
Enrollment
240 participants (actual)
Target follow-up
1 Day
Patient registry
Yes

Groups and cohorts

  • 1.Atrial Fibrillation Group

    Atrial Fibrillation Group: 120 adults aged 60-90 years with documented atrial fibrillation.

  • 2.Control Group

    120 adults aged 60-90 years with no history of atrial fibrillation and documented sinus rhythm.

06

What researchers measure

Primary outcomes

  1. Total Bilateral Jugular Foramen Volume

    Total jugular foramen volume (cm³), calculated as the sum of right and left volumes on archived cranial CT images. Each side is estimated using an elliptical-cylinder model: π/4 × mediolateral diameter × anteroposterior diameter × craniocaudal height, with conversion from mm³ to cm³. Measurements are performed by two readers blinded to group assignment, and their mean is used for analysis. Total volume is compared between participants with atrial fibrillation and controls.

    Time frame: Single time point per participant, using the index cranial CT acquired between January 2022 and July 2026; retrospective assessment without follow-up.

Secondary outcomes

  1. Right and Left Jugular Foramen Volumes

    Right and left jugular foramen volumes (cm³) are assessed separately on archived cranial CT images using an elliptical-cylinder model. Measurements are averaged across two readers blinded to group assignment and compared between participants with atrial fibrillation and controls.

    Time frame: Single time point per participant, using the index cranial CT acquired between January 2022 and July 2026; no longitudinal follow-up.

  2. Discrimination of Atrial Fibrillation by Jugular Foramen Volume

    Discrimination between participants with atrial fibrillation and controls is assessed using the area under the receiver operating characteristic curve (ROC AUC), with 95% confidence intervals, for total bilateral jugular foramen volume and its age- and sex-adjusted z-score.

    Time frame: Retrospective assessment using the index cranial CT and rhythm documentation within 12 months of CT; no longitudinal follow-up.

07

Study locations

1 site
  • Ankara Atatürk Sanatoryum Reseach Training Hospital
    Ankara, 0600, Turkey (Türkiye)
08

References and documents

Individual participant data

Plan to share: No — There is currently no plan to share individual participant data. The study uses retrospective medical records and imaging data, and permission for external data sharing has not been established. Aggregate findings will be reported in scientific publications.

No publications or documents are linked to this record.

09

Timeline

1 registry update since Sep 25, 2026
ElapsedEstimatedEstimated, not yet reached

Ran from Jan 2025 to primary completion in Sep 2026, 20 months.

How these figures are worked out, and which studies are left out of them.

Registered
Nov 2, 2026
First posted
Nov 6, 2026
StartActual
Jan 1, 2025
Primary completionActual
Sep 1, 2026
CompletionActual
Sep 1, 2026
Last update
Nov 6, 2026
What these dates mean
Start.
When the first participant enrolled; while estimated, when the study expects to open to recruitment.
Primary completion.
When the last participant was examined or treated to collect data for the study's main question, its primary outcome. A study that stopped early gives the date its data collection stopped.
Completion.
When the last participant's last visit took place, for every outcome, secondary ones and side effects included: the end of the study. Often later than primary completion, sometimes the same day.
Actual and Est.
Actual means the registry says the date has happened. Est. (estimated) is a date the sponsor plans or expects. It can still move, and the sponsor is expected to change it to actual once it has passed.
Registered
First appeared on the registry. No changes since
Nov 6, 2026
Show all 1 update
  1. Nov 6, 2026
    First appeared on the registry

From the registry record's own update history. This site started tracking changes on Sep 25, 2026; for anything earlier, see the record history on ClinicalTrials.gov ↗

10

Registry details

Key details

Study ID
NCT07922655
Lead sponsor
Ankara Ataturk Sanatorium Training and Research Hospital
Responsible party
Şahbender Koç (Assoc. Prof. Dr., Ankara Ataturk Sanatorium Training and Research Hospital) — Principal investigator
First posted
Nov 6, 2026
Start date
Jan 1, 2025
Primary completion
Sep 1, 2026
Completion
Sep 1, 2026
Last update
Nov 6, 2026

Oversight

Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

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This study is completed, as verified in Nov 2026. You cannot join it, but the record below documents what was studied.

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