Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
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RECRUITING
30 participants
OBSERVATIONAL
2017-10-04
2025-06-30
Brief Summary
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Detailed Description
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Conditions
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Study Design
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COHORT
PROSPECTIVE
Study Groups
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Congenital Diaphragmatic Hernia referred for fetal MRA
No intervention data collected through routine scans
No intervention, we wish to use the images a mother would have done as part of her normal medical care and make both 3D animations and 3D models of the baby and it's CDH.
Interventions
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No intervention data collected through routine scans
No intervention, we wish to use the images a mother would have done as part of her normal medical care and make both 3D animations and 3D models of the baby and it's CDH.
Eligibility Criteria
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Inclusion Criteria
* 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
* Under 18 years of age.
* Unable to complete the fetal MRI process due to either metal implants or claustrophobia.
18 Years
FEMALE
No
Sponsors
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Sheffield Teaching Hospitals NHS Foundation Trust
OTHER
Responsible Party
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Locations
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Jessop Wing Hospital
Sheffield, South Yorkshire, United Kingdom
Countries
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Facility Contacts
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Other Identifiers
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STH19783
Identifier Type: -
Identifier Source: org_study_id
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