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Three-dimensional Scanning of the Chest: a Comparison Between Three Different Imaging Modalities

Three-dimensional Scanning of the Chest: a Comparison Between Three Different Imaging Modalities

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT04279886
Enrollment
15
Registered
2020-02-21
Start date
2020-02-20
Completion date
2020-04-20
Last updated
2020-07-02

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Chest Wall Disorder

Brief summary

Recently, three-dimensional scanning of the torso has been proposed as an alternative for two-view chest radiographies and computed tomography to determine the severity of pectus excavatum without exposure to ionizing radiation. The range of three-dimensional scanning systems is broad with even varying systems being used within hospitals. Most of these scanning systems have been validated for accuracy and reproducibility, no comparison between these systems is known. In addition, severity measures of pectus excavatum, as well as other research outcomes, surgical planning techniques, and analysis methods are based on a single imaging system. It is subsequently essential to determine whether different imaging systems can be used interchangeably regarding accuracy and reproducibility. The aim of this study was to assess the reproducibility and accuracy between three commonly used three-dimensional scanning systems.

Interventions

OTHERThree-dimensional scans

All included healthy volunteers received 6 three-dimensional scans, utilizing 3 different scanning systems (2 scans per system)

Sponsors

Radboud University Medical Center
CollaboratorOTHER
Zuyderland Medisch Centrum
Lead SponsorOTHER

Study design

Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
DIAGNOSTIC
Masking
NONE

Intervention model description

All included healthy volunteers received 6 three-dimensional scans, utilizing 3 different scanning systems (2 scans per system)

Eligibility

Sex/Gender
ALL
Healthy volunteers
Yes

Inclusion criteria

* Healthy volunteers only

Exclusion criteria

* none

Design outcomes

Primary

MeasureTime frameDescription
Reproducibility1 monthMean difference between subsequent scans utilizing the same three-dimensional scanning system
Accuracy1 monthMean difference between scans, acquired by different three-dimensional scanning systems

Countries

Netherlands

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026