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Maternal Outcomes Following Manual Lysis of the Placenta.

RecruitingNAAges 18 Years - 45 YearsFemaleHoly Family Hospital, Nazareth, Israel
NCT03626844 on ClinicalTrials.gov ↗
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In plain words

What the trial is, and whether it could suit you

Comparison of maternal outcomes following manual lysis of placenta 15 vs 30 minutes after delivery. A primary outcome of the drop in hemoglobin will be compared between the two groups. Secondary outcomes include blood transfusion rate, maternal satisfaction, time to first breastfeeding, length of hospital stay, infection rate etc.

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📋 Eligibility rules (as published)
Inclusion Criteria: * Term spontaneous vaginal delivery. * Singleton Pregnancy. * Epidural Analgesia during delivery. * Age between 18 and 45 years. Exclusion Criteria: * Active bleeding after delivery that warrants prompt removal of placenta regardless of time from delivery. * Vacuum Extraction. * Intrapartum Infection. * Intrapartum fever above 38 degrees celsius. * Wide 3rd and 4th degree perineal tears that mandate suturing under general anaesthesia. * Thalassemia Carriers.
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What it tests

  • Manual Lysis of Placenta after 15 minutes (Intervention)
  • Manual Lysis of Placenta after 30 minutes (Control)
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Where

1 site
Holy Family Hospital
Nazareth, Israel
🤝 Taking part is your choice, and you can leave at any time. Only the trial team can confirm you are eligible — always decide together with your own doctor.
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