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 @ 2:00 AM
Ignite Modification Date:
2025-12-25 @ 2:00 AM
NCT ID:
NCT04122794
Eligibility Criteria:
Inclusion Criteria:
* Patients who are attending the Maternity Services who are pregnant and due for routine delivery.
* Aged 18- 40 years.
* Are willing and capable to voluntarily sign a statement of informed consent to take part in this investigation.
* Patients due to give birth to twins will be included in this study. Women having both "normal" delivery and caesarean section delivery will be included in this study.
Exclusion Criteria:
* Patients unable to provide informed consent.
* Patients who are under the age of 18 and over the age of 40 years.
* Patients who are deemed unsuitable due to any circumstances as deemed appropriate by the Consultant.
* Patients with a Blood Borne Virus (HIV Type 1, HIV Type 2, Hepatitis B, Hepatitis C) will be excluded from the study.
* Patients with diabetes that is not gestational in nature will be excluded from this study.
* Patients due to deliver triplets or more will be excluded from this study.
* Patients who deliver their baby before 37 weeks gestation will not have umbilical cord tissue retained for study purposes.
Sex:
FEMALE
Minimum Age:
18 Years
Maximum Age:
40 Years
Study:
NCT04122794
Study Brief:
Protocol Section:
NCT04122794