UnknownNot Applicable

Bilateral Uterine Artery Ligation in PPC Technique for Management of PAS

Egypt130 participantsStarted 2022-04-01

Plain-language summary

Aim of the study Primary outcomes: 1. The effect of bilateral uterine artery ligation in reducing intraoperative bleeding in women underwent PPC as a conservative surgical technique. 2. Decrease surgical time. Secondary outcomes: 1. Associated maternal morbidity and mortality. 2. Amount of blood transfusion 3. Difference in hematocrit value before and after delivery

Who can participate

Age range16 Years – 45 Years

SexFEMALE

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

Inclusion Criteria: * • Previous operations * Gestational age (28 weeks) * Prenatally suspected PAS based on sonographic and/or MRI findings and/or intrapartum diagnosis of PAS. * Authorization to participate in the study Exclusion Criteria: * • Coagulopathies * Chronic renal or hepatic impairment (baseline first trimester labs are beyond normal range for pregnancy) * Delivery in an outside hospital (patients referred for ongoing massive bleeding due to PAS) * Patients coming in emergency condition with bleeding or in labour.

What they're measuring

bilateral uterine artery ligation

Timeframe: 30 months

Trial details

NCT IDNCT05314595

SponsorAssiut University

Sponsor typeOTHER

Study typeINTERVENTIONAL

Primary completion2022-08-01

Contact for this trial

mostafa hussein

01558678842 mostafa.elnazeir1994@gmail.com

View on ClinicalTrials.gov More Placenta Accreta trials