Eligibility Module
The Eligibility Module contains detailed information about who can participate in the clinical trial. This includes eligibility criteria, age restrictions, gender requirements, healthy volunteer status, and study population descriptions, helping researchers understand who is eligible to participate in the study.
Eligibility Module path is as follows:
Study -> Protocol Section -> Eligibility Module
Eligibility Module
Ignite Creation Date:
2025-12-25 @ 3:27 AM
Ignite Modification Date:
2025-12-25 @ 3:27 AM
NCT ID:
NCT06259305
Eligibility Criteria:
Inclusion Criteria:
* · Pregnant people aged 18 and over
* Experiencing a pregnancy where, due to a foetal diagnosis, the baby is unlikely to survive to full term or a comfort care only plan for postnatal care has been agreed between the parents and the health care professionals
* Subjects capable of giving informed consent
* Subjects have sufficient comprehension of the English language to enable informed consent
* Subjects have, or can get, a recording of their baby's heartbeat that they are willing to share with the PI for the purpose of the study
Exclusion Criteria:
* · Pregnant people \<18 years of age
* Lack of capacity to provide informed consent
* Have insufficient comprehension of the English Language to provide informed consent
* No recording of baby's heartbeat, and not able to get one, or not willing to share with the PI for the purpose of the study
Healthy Volunteers:
False
Sex:
FEMALE
Minimum Age:
18 Years
Study:
NCT06259305
Study Brief:
Protocol Section:
NCT06259305