Last updated: May 1, 2024
Sponsor: Assiut University
Overall Status: Active - Recruiting
Phase
N/A
Condition
Preeclampsia
Pregnancy Complications
Treatment
fetal ultrasound
Clinical Study ID
NCT06395974
Fetal renal a./preeclampsia
Female Accepts Healthy Volunteers
Study Summary
Eligibility Criteria
Inclusion
Inclusion Criteria:
- a) Preeclampsia:
- Women with preeclampsia >28 weeks of pregnancy.
- Singleton pregnancy.
- Women with intrauterine growth restriction and abnormal amniotic fluid volume tosimulate real world data. b) Control:
- Women with healthy pregnancy matched by closest gestational age.
Exclusion
Exclusion Criteria:
- ● Multiple pregnancy.
- Known Congenital fetal malformations.
- Women with other comorbidity such as ischemic heart disease, DM, Autoimmunedisorders, kidney disease, neurological disorders, liver or haematologicaldisorders.
- Women unable to provide informed consent.
- Women who refuse to participate
Study Design
Total Participants: 88
Treatment Group(s): 1
Primary Treatment: fetal ultrasound
Phase:
Study Start date:
November 01, 2023
Estimated Completion Date:
December 31, 2024
Study Description
Connect with a study center
Assiut university hospital
Assiut,
EgyptActive - Recruiting
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