CompletedPhase 2

Efficacy Study of Random Placenta Margin Incision to Treat Complete Placenta Previa

China100 participantsStarted 2016-01

Plain-language summary

The purpose of this study is to assess the efficacy of random placenta margin incision for hemorrhage control during cesarean section of complete placenta previa pregnancies.

Who can participate

Age range18 Years – 45 Years

SexFEMALE

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Inclusion Criteria: * A gestation age of ≥ 28 weeks * Delivered by cesarean section * Antepartum diagnosis of complete placenta accreta by obstetric ultrasound and doppler Exclusion Criteria: * Women who refuse to participate * Pregnant women with serious diseases

What they're measuring

Postpartum Hemorrhage

Timeframe: within the first 30 days after cesarean section

Trial details

NCT IDNCT02695069

SponsorMaternal and Child Health Hospital of Foshan

Sponsor typeOTHER

Study typeINTERVENTIONAL

Primary completion2017-03

View on ClinicalTrials.gov More Complete Placenta Previa trials