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 @ 12:22 AM
Ignite Modification Date:
2025-12-25 @ 12:22 AM
NCT ID:
NCT05199558
Eligibility Criteria:
Inclusion Criteria:
1. Eclampsia:
* Diagnosed as new onset generalized tonic colonic seizures or coma in pregnant women or women who have recently given birth.
* Singleton pregnancies.
* All gestational ages, including post-partum eclampsia
* Enrolment to the study must occur within 7 days of an eclamptic episode Women must be coherent and able to provide informed consent prior to enrolment
2. Preeclampsia:
● Diagnosed as new onset of hypertension (\>140 mmHg systolic or \> 90 mmHg diastolic) after the 20th week of gestation and the coexistence of one or more of the following new onset conditions:Proteinuria ,Other maternal organ evolvement.
* Singleton pregnancy.
* Have not experience an eclamptic episode
3. Normotensive controls:
* Healthy normotensive pregnant woman recruited from women seeking maternity services during the same or similar period
* Matched 1:1 for each eclampsia and preeclampsia case
* Matched by closest gestational age at recruitment to cases and parity
Exclusion Criteria:
* Women with multiple pregnancies.
* Women with seizures attributed to a diagnosis other than eclampsia such as; central nervous system infections, a history of seizures or epilepsy, medications and/or illicit drug use.
* Women unable to provide informed consent
Healthy Volunteers:
True
Sex:
FEMALE
Minimum Age:
15 Years
Maximum Age:
45 Years
Study:
NCT05199558
Study Brief:
Protocol Section:
NCT05199558