RecruitingNCT05802251

Sonographic Parameters and Risk of Antepartum Hemorrhage in Asymptomatic Women With Placenta Previa: A Cohort Study

Sponsor

Ain Shams University

Enrollment

68 participants

Start Date

Jun 1, 2022

Study Type

OBSERVATIONAL

Conditions

Placenta Previa

Summary

The aim of this study is to evaluate the effectiveness of ultrasonographic parameters (cervical length, placental thickness and distance placental edge from internal os of the cervix) in predicting the risk of antepartum hemorrhage and emergency cesarean delivery in asymptomatic women with placenta previa.

Eligibility

Sex: FEMALE

Plain Language Summary

Simplified for easier understanding

This clinical trial is studying Ultrasonographic parameters for people with placenta previa. The study is currently recruiting participants at 1 location. People eligible for this study include women.

This summary was AI-generated to explain the trial in plain language. It is not medical advice. Always discuss eligibility with your doctor before enrolling in a clinical trial.

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Interventions

DIAGNOSTIC_TESTUltrasonographic parameters

cervical length. placental thickness. distance placental edge from internal os of the cervix

Locations(1)

Faculty of Medicine, Ain Shams University

Cairo, Egypt

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NCT05802251

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