CompletedPhase 2/3

the Treatment of Postpartum Hemorrhage Due to Placenta Previa Complete Centralis

Egypt50 participantsStarted 2012-07

Plain-language summary

Objective: To assess the efficacy of lower uterine compression sutures (involved bilateral uterine artery ligation and compression of the lower uterine segment at the same time with one circular stitch) as a conservative treatment for the treatment of postpartum hemorrhage in women with placenta previa complete centralis. Method: This prospective study of 50 women with postpartum hemorrhage following removal of placenta previa complete centralis during elective cesarean section. All 50 patients will have lower uterine compression sutures (involving bilateral uterine artery ligation and compression of the lower uterine segment at the same time with one circular stitch). All patients will be followed postpartum for evaluation of uterine cavity and menstrual cycles

Who can participate

Age range21 Years – 46 Years

SexFEMALE

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Inclusion Criteria: * a gestation age of ≥ 28 weeks and antepartum hemorrhage; * intraoperative postpartum hemorrhage and discovery of a placenta previa; * successful removal of the placenta Exclusion Criteria: * shock due to massive blood loss * failure of successful removal of the placenta

What they're measuring

Treatment of Postpartum Hemorrhage

Timeframe: during cesarean section( participants will be followed for the duration of hospital stay)

Trial details

NCT IDNCT02157441

SponsorBenha University

Sponsor typeOTHER

Study typeINTERVENTIONAL

Primary completion2015-09

View on ClinicalTrials.gov More Placenta Previa Complete Centralis trials