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Study of Late-foetal Human Organ Development

Study of Late-foetal Human Organ Development

Status
Recruiting
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT04661059
Enrollment
2000
Registered
2020-12-09
Start date
2022-02-03
Completion date
2040-12-31
Last updated
2023-12-05

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

Conditions

Congenital Disorders

Brief summary

Knowledge about abnormal organ development is important to understand pathology and to develop novel treatment approaches for individuals with congenital and acquired disease. Most of our current understanding is based on examination of tissues from the embryo and early fetus, collected from women undergoing termination of pregnancy in the first trimester (third) of pregnancy. There is very little known about normal and abnormal organ development from a developmental perspective during the crucial last two-thirds of pregnancy when much remodelling of fetal tissues occurs. We aim to collect tissue from a variety of developing fetal organs in the last two-thirds of pregnancy from women who decide to undergo a termination of pregnancy and who wish to undergo a clinical fetal postmortem (PM) examination.

Interventions

None listed

Sponsors

University College London Hospitals
Lead SponsorOTHER

Study design

Observational model
CASE_ONLY
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum

Inclusion criteria

* ≥18 years old pregnant women who attend the Fetal Medicine Unit for concerns about a fetal abnormality where they decide to proceed to termination of pregnancy

Exclusion criteria

* Screening labs positive for maternal HIV, Hepatitis B and Hepatitis C, Chlamydia and Herpes. * Subject unable to make an informed decision about termination of pregnancy.

Design outcomes

Primary

MeasureTime frameDescription
Cellular maturityImmediately after tissue collectionImmunofluorescence staining

Countries

United Kingdom

Contacts

Primary ContactSarah Gibbon
sarah.gibbon1@nhs.net+44 20 3456 7890

Outcome results

None listed

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