Actively Recruiting

Age: 18Years +
All Genders
ID04661059

Study of Late-foetal Human Organ Development

Led by University College London Hospitals · Updated on 2023-12-05

2000

Participants Needed

1

Research Sites

848 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

Understanding abnormal organ development is crucial for improving knowledge of congenital and acquired diseases and for developing new treatments. Most current insights come from examining tissues from early pregnancy terminations, but little is known about organ development during the last two-thirds of pregnancy, a key period when fetal tissue remodeling occurs. This study aims to collect tissue samples from various fetal organs during this late stage of pregnancy from women undergoing termination who agree to a fetal postmortem examination. The study is observational and focuses on collecting and analyzing fetal tissue samples. There are no interventions or treatments being tested. The tissue collection occurs after termination of pregnancy during a clinical fetal postmortem examination. The main focus is on assessing cellular maturity immediately after tissue collection to better understand late fetal organ development. Participants will be pregnant women aged 18 years or older who decide to terminate their pregnancy due to fetal abnormalities and consent to postmortem tissue collection. Researchers will gather tissue samples and analyze cellular maturity. Safety and ethical considerations include the consent process and screening for infections. The study will continue until December 31, 2040, with data collected and analyzed to advance knowledge of fetal organ development.

CONDITIONS

Brief Title

Study of Late-foetal Human Organ Development

Who Can Participate

Age: 18Years +
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Pregnant women aged 18 years or older who attend the Fetal Medicine Unit for concerns about fetal abnormality and decide to proceed with termination of pregnancy
Not Eligible

You will not qualify if you...

  • Positive screening tests for maternal HIV, Hepatitis B, Hepatitis C, Chlamydia, or Herpes
  • Unable to make an informed decision about termination of pregnancy

AI-Screening

AI-Powered Screening

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Your Study Journey

Screening

Duration - 2 to 4 weeks

Participants are screened for eligibility to participate in the trial.

Trial Site Locations

Total: 1 location

1

University College Hospitals NHS Foundation Trust

London, United Kingdom

Actively Recruiting

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Research Team

S

Sarah Gibbon

How is the study designed?

Study Type

OBSERVATIONAL

Masking

N/A

Allocation

N/A

Model

N/A

Primary Purpose

N/A

Number of Arms

0

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