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Clinical Trial Details — Status: Recruiting

Administrative data

NCT number NCT03926078
Other study ID # METCZ20190048
Secondary ID
Status Recruiting
Phase N/A
First received
Last updated
Start date August 21, 2019
Est. completion date March 2021

Study information

Verified date July 2020
Source Zuyderland Medisch Centrum
Contact Jean Daemen
Phone +31884597777
Email j.daemen@zuyderland.nl
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

Pectus excavatum (PE) is the most common anterior chest wall deformity. Currently, a chest radiography (CR) or Computed Tomography (CT) scan is acquired to determine and objectify pectus severity using the Haller Index. Alongside other determinants, the Haller Index value is used in the proces of clinical decision making and determine surgical candidacy. However, cross-sectional imaging based calculation of the Haller Index implies exposure to ionizing radiation that should be limited at all times to diminish the cumulative long-term risks of malignancy. Especially in pectus patients that often concerns children.

Three-dimensional (3D) optical surface imaging offers a non-invasive, radiation-free alternative that may be used to obtain thoracic measures and determine pectus severity. However, for 3D images/scans to be used as a diagnostic tool in the proces of clinical decision making and determine surgical candidacy, its diagnostic accuracy should be evaluated. This will be investigated utilizing a pilot study design as no prior accuracy studies are available.


Description:

This single-centre prospective pilot study is conducted to assess the diagnostic accuracy of 3D optical surface imaging based external Haller Index (EHI) measurements to quantify the severity of pectus excavatum. CR and CT based conventional Haller Indices (HI) are used as reference method.

CR and CT are both used as reference method, as the work-up of pectus patients in our centre is dependent of age. Subsequently, two groups are created: (A) patients under 18 years of age that receive a frontal (anteroposterior) and sagittal chest radiography, and (B) patients aged 18 years or older that receive a chest CT scan.

In this study, patients are their own control. To obtain optical surface images, a handheld 3D scanner is used. During acquisition, subjects will be standing in an upright position with arms abducted. Standard routinely used protocols are used to acquire chest radiographies and CT scans.

The HI is obtained from all chest radiographies and CT scans, calculated by dividing the widest thoracic transverse diameter by the anteroposterior distance, measured from the posterior surface of sternum to the anterior surface of the vertebral body. The EHI, a modified measurement to assess pectus deformity, is used to quantify PE severity based on 3D optical surface images. The EHI is calculated by dividing the widest external thoracic transverse diameter by the distance between the external deepest point or point of maximal protrusion and external vertebral body. The EHI is also calculated from the available chest radiographies and CT scans.

All measurements will be performed by three blinded observers that are not responsible to perform a comprehensive interpretation of the study. Following acquisition of all indices, the inter-observer reliability is calculated using the intraclass correlation coefficient. Based on the means, a receiver-operating characteristic (ROC)-curve is created for the 3D scan based EHI measurements, utilizing the surgical indication based on CR and CT (HI larger or equal to 3.25) images as gold standard. The optimal cut-off value, obtained from the ROC-curve is subsequently used to determine the 3D optical surface images' diagnostic accuracy.


Recruitment information / eligibility

Status Recruiting
Enrollment 28
Est. completion date March 2021
Est. primary completion date February 2021
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group N/A and older
Eligibility Inclusion criteria:

- All patients that visit the Zuyderland Medical Centre outpatient clinic for evaluation of their pectus excavatum.

- No age restrictions were imposed, however, to be eligible, it was mandatory to be able to stand still in and upright position for 60 seconds.

Exclusion criteria:

- Patients that suffer from any form of light hypersensitivity or epilepsy were not considered while 3D optical surface images were acquired with the use of structured, flashing light.

Study Design


Related Conditions & MeSH terms


Intervention

Other:
3D optical surface image
3D optical surface images will be acquired and used to calculate the EHI
Radiation:
Chest radiography
Chest radiographies will be acquired and used to calculated the HI and EHI
CT scan
CT scans will be acquired and used to calculate the HI and EHI

Locations

Country Name City State
Netherlands Zuyderland Medical Centre Heerlen Limburg

Sponsors (1)

Lead Sponsor Collaborator
Zuyderland Medisch Centrum

Country where clinical trial is conducted

Netherlands, 

Outcome

Type Measure Description Time frame Safety issue
Primary Diagnostic accuracy of the EHI, calculated from 3D optical surface images Dependent of age, the CR or CT based HI is utilized as reference method 1 year
Secondary Inter-observer reliability Inter-observer reliability of CR, CT and 3D image derived (external) Haller Inidices, obtained by 3 observers 1 year
Secondary Correlation of CT scan derived HI and EHI Correlation is assessed by the Pearson's correlation coefficient 1 year
Secondary Correlation of CT scan derived EHI and 3D optical surface image derived EHI Correlation is assessed by the Pearson's correlation coefficient 1 year
Secondary Correlation of CT and CR derived HI with 3D optical surface image derived EHI Correlation is assessed by the Pearson's correlation coefficient 1 year
Secondary Absolute agreement of CT scan derived EHI and 3D optical surface image derived EHI Assessed by the intraclass correlation coefficient 1 year
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