Actively Recruiting

Age: 18Years +
FEMALE
ID03750266

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.

Led by Sheffield Teaching Hospitals NHS Foundation Trust · Updated on 2025-05-16

30

Participants Needed

1

Research Sites

N/A

Total Duration

On this page

AI-Summary

What this Trial Is About

This research focuses on pregnant women whose unborn babies have been diagnosed with Congenital Diaphragmatic Hernia (CDH), a condition where a hole in the diaphragm allows organs to move into the chest. The study aims to use images taken during routine medical care to create 3D animations and models of the baby and the CDH. These models help parents understand the condition and assist surgeons in planning surgery after birth. The study involves using existing routine scans from pregnant women referred for fetal MRI without any additional intervention. Researchers will create detailed 3D visualizations from these images to better illustrate the size of the diaphragmatic hole and the position of the organs. The study includes patients from diagnosis through to the post-operative period after birth. Participants will be pregnant women attending a fetal medicine unit who have agreed to take part. Researchers will collect baseline information such as patient demographics. The study observes the use of 3D imaging to support clinical management and surgical planning. Participation involves no additional treatment, only the use of images already taken during standard prenatal care. The study is ongoing and will continue until June 2025.

CONDITIONS

Brief Title

3D Animation and Models to Aid Management of Fetal CDH

Who Can Participate

Age: 18Years +
FEMALE

Eligibility Criteria

Eligible

You may qualify if you...

  • Pregnant women attending Jessop Wing Fetal medicine unit
  • Fetus diagnosed with Congenital Diaphragmatic Hernia (CDH) and referred for fetal MRI
  • Pregnant women who agree to take part in the study
Not Eligible

You will not qualify if you...

  • Unable 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 metal implants or claustrophobia

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Your Study Journey

Screening

Duration - 2 to 4 weeks

Participants are screened for eligibility to participate in the trial.

1 visit (in-person)

Monitoring

Duration - From diagnosis through the post-operative period

Participants who undergo routine scans are observed with 3D images and models created from routine fetal MRI and ultrasound data.

Visits occur as part of routine medical care

Trial Site Locations

Total: 1 location

1

Jessop Wing Hospital

Sheffield, South Yorkshire, United Kingdom, S10 2JF

Actively Recruiting

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How is the study designed?

Study Type

OBSERVATIONAL

Masking

N/A

Allocation

N/A

Model

N/A

Primary Purpose

N/A

Number of Arms

1

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