Using 3D models to help manage congenital diaphragmatic hernia in fetuses
The Role of 3D Images and Models to Aid Management of Cases of Congenital Diaphragmatic Hernia Diagnosed in the Antenatal Period. Consecutive Patients Studied From Diagnosis to Post Operative Period.
This study is trying to use 3D models made from MRI scans to help parents and doctors better understand and plan for surgery for fetuses with congenital diaphragmatic hernia.
Quick facts
| Study type | Observational |
|---|---|
| Enrollment | 30 (estimated) |
| Ages | 18 Years and up |
| Sex | Female |
| Sponsor | Sheffield Teaching Hospitals NHS Foundation Trust Academic / other |
| Locations | 1 site (Sheffield, South Yorkshire) |
| Trial ID | NCT03750266 on ClinicalTrials.gov |
What this trial studies
This observational study aims to create 3D animations and models of fetuses diagnosed with congenital diaphragmatic hernia (CDH) using routine medical imaging. By visualizing the size of the defect and the positioning of organs, the study seeks to enhance understanding for both parents and surgical teams. The approach leverages existing MRI scans to provide detailed insights without any additional interventions. This method could improve preoperative planning and parental education regarding the condition.
Who should consider this trial
Good fit: Ideal candidates are pregnant women attending the Jessop Wing Fetal Medicine Unit whose fetuses have been diagnosed with CDH and are referred for MRI.
Not a fit: Patients who may not benefit include those unable to provide informed consent, under 18 years of age, or unable to undergo MRI due to claustrophobia or metal implants.
Why it matters
Potential benefit: If successful, this could lead to better surgical outcomes and improved understanding of CDH for families.
How similar studies have performed: While the use of 3D modeling in medical imaging is gaining traction, this specific application for CDH management is relatively novel and has not been extensively tested in prior studies.
Eligibility criteria
Show full inclusion / exclusion criteria
Inclusion Criteria: * Target Population: pregnancy women attending Jessop Wing Fetal medicine unit. * Accessible population: Pregnant women attending Jessop Wing Fetal medicine unit. Whose fetus had a CDH and are referred to MRI. * Study population: Pregnant women attending Jessop Wing Fetal medicine unit. Whose fetus had a CDH and are referred to MRI and agree to take part in the study. Exclusion Criteria: * Not able to give informed consent due to any reason including poor understanding of English * Under 18 years of age. * Unable to complete the fetal MRI process due to either metal implants or claustrophobia.
Where this trial is running
Sheffield, South Yorkshire
- Jessop Wing Hospital — Sheffield, South Yorkshire, United Kingdom (Recruiting)
How to participate
- Review the eligibility criteria above with your treating physician.
- Visit the official trial page on ClinicalTrials.gov for the most current contact information and recruitment status.
- Contact the listed study coordinator or principal investigator to request pre-screening. Pre-screening is free and never obligates you to enroll.