Anatomical Assessment of Orbital Contents on Imaging (EACOI) (EACOI)

January 16, 2026 updated by: University Hospital, Brest

Anatomical Assessment of Orbital Contents on Imaging

This is a single-center retrospective study based on existing data. The study focuses on the anatomical content of the orbit, and in particular the anatomy of the oculomotor muscles in the orbit, which are involved in eye movements. There are 6 of these muscles, with the superior, inferior, medial and lateral rectus muscles, and the superior and inferior oblique muscles in each orbit. The study also covers the anatomy of the optic nerve and orbital fat.

Knowledge of the anatomy and biometry of the oculomotor muscles, and of methods for assessing these muscles, has implications for clinical, medical and surgical practice.

Study Overview

Status

Recruiting

Conditions

Study Type

Observational

Enrollment (Estimated)

190

Contacts and Locations

This section provides the contact details for those conducting the study, and information on where this study is being conducted.

Study Contact

Study Locations

      • Brest, France, 29609
        • Recruiting
        • CHU Brest

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Eligibility Criteria

Ages Eligible for Study

  • Adult
  • Older Adult

Accepts Healthy Volunteers

Yes

Sampling Method

Non-Probability Sample

Study Population

Patients in the general population who underwent brain imaging (CT or MRI) in the medical imaging department

Description

Inclusion Criteria:

  • Patients over 18
  • No opposition to the participation
  • Usable imaging test

Exclusion Criteria:

  • Refusal to participate

Study Plan

This section provides details of the study plan, including how the study is designed and what the study is measuring.

How is the study designed?

Design Details

Cohorts and Interventions

Group / Cohort
Oculomotor muscles study
Intraorbital content

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Intra- and inter-observer reproducibility of oculomotor muscle anatomical criteria in imaging
Time Frame: 1 year.
Evaluate the reproducibility of different oculomotor muscle measurements, such as volume (mm3), surface (mm2) or two-dimensional measurements (mm). Differences to the mean. Intraclass correlation coefficient (ICC).
1 year.

Secondary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Reproducibility of measurements of optic nerve size and orbital fat in imaging
Time Frame: 1 year.
Evaluate the reproducibility of different measurements to assess the size of the optic nerve (volume (mm3), surface (mm2), two-dimensional measurement (mm) and intra-orbital fat (mm3). Dfference to the mean. Intraclass correlation coefficient (ICC).
1 year.

Collaborators and Investigators

This is where you will find people and organizations involved with this study.

Study record dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Major Dates

Study Start (Actual)

May 1, 2024

Primary Completion (Estimated)

June 30, 2026

Study Completion (Estimated)

June 30, 2026

Study Registration Dates

First Submitted

June 3, 2025

First Submitted That Met QC Criteria

January 16, 2026

First Posted (Actual)

January 22, 2026

Study Record Updates

Last Update Posted (Actual)

January 22, 2026

Last Update Submitted That Met QC Criteria

January 16, 2026

Last Verified

January 1, 2025

More Information

Terms related to this study

Other Study ID Numbers

  • 29BRC23.0315 - EACOI

Plan for Individual participant data (IPD)

Plan to Share Individual Participant Data (IPD)?

UNDECIDED

Drug and device information, study documents

Studies a U.S. FDA-regulated drug product

No

Studies a U.S. FDA-regulated device product

No

This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.

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