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Preliminary Study of Pediatric Diaphragmatic Elastography

Ultrasound Functional Analysis of the Diaphragm and Upper Digestive Tract in Patients with Congenital Diaphragmatic Hernia

Status
Not yet recruiting
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT06666140
Acronym
ECHODIA
Enrollment
80
Registered
2024-10-30
Start date
2024-11-15
Completion date
2027-11-15
Last updated
2024-10-30

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

Conditions

Congenital Diaphragmatic Hernia

Keywords

congenital diaphragmatic hernia, ultrasound elastography, Chronic respiratory diseases, pulmonary hypertension, hypoplasia

Brief summary

This diaphragmatic elastography study is a preliminary pilot study to have first values of diaphragmatic stiffness in patients with a history of diaphragmatic hernia and to estimate the difference in stiffness compared to a group of patients without a history of hernia. The hypothesis is to be able to correlate the values found with the patients' symptomatology and thus to better monitor patients by a simple, accessible, painless and reproducible diagnostic tool, to better understand their evolution and even to be able to anticipate possible difficulties (reflux, respiratory disorders, scoliosis, etc.). Ultrasound elastography is a recent and clinically recognized method that uses an ultrasound approach to determine tissue stiffness in a non-invasive way.

Interventions

The measurement of diaphragmatic stiffness by shear waves is performed with a high-frequency linear ultrasound probe, intercostally, during apneas lasting a few seconds. After quantitative diaphragm thickness measurements, the ultrasound probe positioning is unchanged and regions of interest are placed in the patient's diaphragm thickness as well as in the adjacent liver or spleen (baseline). A stiffness result is obtained in kPa. The elastography measurement extends the duration of the ultrasound scheduled as part of patient care by only 10 minutes. The examination is painless and non-invasive.

Sponsors

University Hospital, Strasbourg, France
Lead SponsorOTHER

Study design

Allocation
NON_RANDOMIZED
Intervention model
PARALLEL
Primary purpose
DIAGNOSTIC
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
3 Years to 17 Years
Healthy volunteers
No

Inclusion criteria

* Group HDC: * Patient followed at the CCMR (centres de compétence maladies rares) HDC of the Strasbourg University Hospital * Aged between 3 and 17 years old inclusive * Indifferent Sex * Subject affiliated to a social protection health insurance scheme or beneficiary of such a scheme * Subject able to understand the objectives and risks of the research and to provide dated and signed informed consent * Subject who has been informed of the results of the preliminary medical examination Control group: * Subject followed in pediatric surgery * Aged between 3 and 17 years old inclusive * Indifferent Sex * Subject affiliated to a social protection health insurance scheme or beneficiary of such a scheme * Subject able to understand the objectives and risks of the research and to provide dated and signed informed consent * Subject who has been informed of the results of the preliminary medical examination

Exclusion criteria

* Group HDC: * Refusal * Language barrier * Diaphragmatic surgery within the last 3 months * Patient with a viral picture in progress at the time of examination (assessment by the investigator) * Patient treated with muscle relaxant * Inability to give the subject informed information (subject in an emergency situation, difficulties in understanding the subject, etc.) * Subject under safeguard of justice * Subject under guardianship or curatorship * Pregnant or breastfeeding woman Control group: * Patient without thoracic pathology * Refusal * Language barrier * Diaphragmatic pathology * Any myopathy * History of surgery of the upper digestive tract (esophagus and/or gastric and/or duodenal) * Patient on muscle relaxant * Patient with a viral picture in progress at the time of examination (assessment by the investigator) * Patient treated with muscle relaxant * Inability to give the subject informed information (subject in an emergency situation, difficulties in understanding the subject, etc.) * Subject under safeguard of justice * Subject under guardianship or curatorship * Pregnant or breastfeeding woman

Design outcomes

Primary

MeasureTime frameDescription
To estimate the difference in diaphragm stiffness between a group of children with a diaphragmatic hernia with or without a prosthesis and a group of children without any diaphragmatic pathology.BaselineDiaphragmatic rigidity in ultrasound elastographic analysis: measurement of diaphragm stiffness in shear wave elastography, in apnea (measurement in kPa).

Secondary

MeasureTime frameDescription
To estimate the difference in diaphragm stiffness between a group of children with a diaphragmatic hernia with a prosthesis and a group of children with a diaphragmatic hernia without a prosthesis.BaselineBilateral measurements for each subject of the diaphragm performed in mode B, Intercostal analysis in mode B
To evaluate the correlation between age and the different parameters measured by ultrasound (on the total population and then within the 3 groups: no hernia, hernia with plaque, hernia without plaque)BaselineCollection of age and the various parameters measured by ultrasound (diaphragmatic thickness and rigidity).
To estimate the association between patient stiffness and symptomatology in HDC subjects.BaselineMeasurement of rigidity and collection of symptoms

Other

MeasureTime frameDescription
To estimate the difference in diaphragmatic mobility between a group of children with a diaphragmatic hernia (with or without a prosthesis) and a group of children without a herniaBaselineMeasurement of diaphragmatic mobility in a group of children with a diaphragmatic hernia (with or without a prosthesis) and a group of children without a hernia
To estimate the difference in pyloric position between a group of children with a diaphragmatic hernia (with or without a prosthesis) and a group of children without a herniaBaselineEvaluation of the position of the pyloric (in strict axial section passing through the hepatic hilum, pylora normally visible. Estimate its position in cm (cranio caudal) in relation to the hilum if not in place) in a group of children with a diaphragmatic hernia (with or without a prosthesis) and a group of children without a hernia
To estimate the association between the absence of the prosthesis and the symptomatology of patients in HDC subjectsBaselineCollection of the presence of a prosthesis and the various symptoms

Countries

France

Contacts

Primary ContactIsabelle TALON
isabelle.TALON@chru-strasbourg.fr+33388127296

Outcome results

None listed

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