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Prostasin Levels in Preeclamptic Women | Clinical Trials | Clareo Health

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COMPLETEDNCT06623942

Prostasin Levels in Preeclamptic Women

This study will aim to compare maternal serum prostasin levels between women diagnosed with preeclampsia and healthy normotensive pregnant controls. Participants will be divided into two main groups: ...

Lead sponsor: Başakşehir Çam & Sakura City Hospital•1 locations•View source on ClinicalTrials.gov

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Sponsors

Lead Sponsor

Başakşehir Çam & Sakura City Hospital

Age

18 - 40 years

Sex

FEMALE

Healthy Volunteers

Yes

Inclusion Criteria

•Diagnosis of Preeclampsia: Defined by new-onset hypertension (systolic Blood Pressure ≥140 mmHg and/or diastolic Blood Pressure ≥90 mmHg) after 20 weeks of gestation, with or without proteinuria.
•Control Group: Healthy pregnancies without preeclampsia or other significant maternal or fetal complications.

Exclusion Criteria

•Multiple Pregnancies
•Pregestational Diabetes
•Chronic Hypertension
•Systemic Diseases (Chronic kidney disease, autoimmune diseases)
•Fetal Anomalies
•Premature Rupture of Membranes.

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Data from ClinicalTrials.govLast updated on ClinicalTrials.gov: October 2, 2024Terms

Trial snapshot

StatusCOMPLETED

Phase—

Enrollment88

Start dateJan 2023

Last updatedOct 2, 2024

Condition

Locations shown

Cam and Sakura City Hospital

Istanbul

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Data Source & Attribution

This clinical trial information is sourced from ClinicalTrials.gov, a service of the U.S. National Institutes of Health.

ClinicalTrials.gov last update: October 2, 2024Data synced to Clareo: May 10, 2026

Modifications: This data has been reformatted for display purposes. Eligibility criteria have been parsed into inclusion/exclusion sections. Location data has been geocoded to enable distance-based search. For the authoritative and most current information, please visit ClinicalTrials.gov.

Neither the United States Government nor Clareo Health make any warranties regarding the data. Check ClinicalTrials.gov frequently for updates.

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