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Clinical Trials/NCT06666140
NCT06666140
Not yet recruiting
Not Applicable

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

University Hospital, Strasbourg, France1 site in 1 country80 target enrollmentNovember 15, 2024

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Congenital Diaphragmatic Hernia
Sponsor
University Hospital, Strasbourg, France
Enrollment
80
Locations
1
Primary Endpoint
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.
Status
Not yet recruiting
Last Updated
last year

Overview

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.

Registry
clinicaltrials.gov
Start Date
November 15, 2024
End Date
November 15, 2027
Last Updated
last year
Study Type
Interventional
Study Design
Parallel
Sex
All

Investigators

Sponsor
University Hospital, Strasbourg, France
Responsible Party
Sponsor

Eligibility Criteria

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

Exclusion Criteria

  • Group HDC:
  • 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:

Outcomes

Primary Outcomes

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.

Time Frame: Baseline

Diaphragmatic rigidity in ultrasound elastographic analysis: measurement of diaphragm stiffness in shear wave elastography, in apnea (measurement in kPa).

Secondary Outcomes

  • 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.(Baseline)
  • 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)(Baseline)
  • To estimate the association between patient stiffness and symptomatology in HDC subjects.(Baseline)

Study Sites (1)

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