UnknownNot Applicable

Combined Bilateral Uterine Artery Ligation and Bakri Balloon During Cesarean Section

Egypt150 participantsStarted 2020-09-01

Plain-language summary

This study will be performed to compare the effectiveness of routine Bakri balloon tamponade and Bilateral Uterine Artery Ligation during cesarean section in patients with placenta previa

Who can participate

Age range18 Years – 45 Years

SexFEMALE

See this in plain English?

AI-rewrites the medical criteria so a patient or caregiver can understand them. Always confirm with the trial site.

Inclusion Criteria: * women undergoing elective cesarean delivery for complete placenta previa which not respond uterotonic and simple hemostatic maneuvers like placental bed hemostatic sutures Exclusion Criteria: * patients with the high possibility of morbid adherent placenta * those presented with severe antepartum hemorrhage * Patients with cardiac, hepatic, renal, or thromboembolic disease; * patient refuses to consent

What they're measuring

mean Blood loss after placental separation

Timeframe: 30 minutes

Trial details

NCT IDNCT04518150

SponsorAswan University Hospital

Sponsor typeOTHER

Study typeINTERVENTIONAL

Primary completion2022-08-31

Contact for this trial

hany f Sallam, md

+20102435461 hany.farouk@aswu.edu.eg

View on ClinicalTrials.gov More Placenta Previa trials