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Recruiting

NCT Number: NCT04895891

3D Personalized Modelization of the Hand Using EOS Imaging System

This study aims to compare the quality of 3D hand modelization with EOS imaging with gold-standard computed tomography

Recruiting

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Key information

Age range

18 year and older

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

CHU de Besançon

Besançon, France

Location status: Recruiting

Location contact

François Loisel, MD

CONTACT

François Loisel, MS

PRINCIPAL_INVESTIGATOR

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Patient with hand/wrist CT required
  • Informed consent form signed

Treatment and study plan

EOS hand imaging

Device

For each patient, EOS images are compared with CT images

Primary outcomes

  1. Data obtained through EOS imaging

    Time frame: Day 60

    Precision and correlation of the 3D modelization of hand is compared between the two imaging methods

  2. Data obtained through standard CT

    Time frame: Day 60

    Precision and correlation of the 3D modelization of hand is compared between the two imaging methods

Study contacts

Contact information is provided by the study sponsor or research team.

François Loisel, MD

CONTACT

[email protected]

0033381667540

Sponsors and collaborators

Lead sponsor

Centre Hospitalier Universitaire de Besancon

Other

Registry information

Acronym: M3DME

Important dates

Study start
2020
Primary completion
2025
Study completion
2025
First posted
May 20, 2021
Registry last updated
Sep 19, 2024

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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