Status:

UNKNOWN

Improved Characterisation of Eclampsia

Lead Sponsor:

Assiut University

Conditions:

Eclampsia Preeclampsia

Eligibility:

FEMALE

15-45 years

Brief Summary

Eclampsia is a serious pregnancy complication.In our study we aim to characterize the clinical signs and symptoms that occur prior to the onset of eclampsia in a prospectively collected cohort.And Com...

Detailed Description

Eclampsia is a serious pregnancy complication that occurs when a pregnant woman - or new mother - experiences seizures associated with hypertension. These seizures pose a major risk to the life and th...

Eligibility Criteria

Inclusion

  • 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
  • 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
  • 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

  • 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

Key Trial Info

Start Date :

March 1 2022

Trial Type :

OBSERVATIONAL

Allocation :

ESTIMATED

End Date :

December 1 2024

Estimated Enrollment :

1200 Patients enrolled

Trial Details

Trial ID

NCT05199558

Start Date

March 1 2022

End Date

December 1 2024

Last Update

February 16 2022

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