Clinical Trial

Maternal Outcomes Following Manual Lysis of the Placenta.

Not Yet Recruiting
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Summary
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.
Protocol Amendment History 3 amendments
This ClinicalTrials.gov record has been amended 3 times since 2018-08-08; most recent amendment 2026-07-03.
Status change: Suspended → Not Yet Recruiting 2026-07-03
Status change: Recruiting → Suspended 2020-02-12
Status change: Not Yet Recruiting → Recruiting 2018-11-21
Trial Details
NCT Number NCT03626844
Lead Sponsor Holy Family Hospital, Nazareth, Israel
Conditions Third Stage of Delivery
Enrollment 100 participants
Start Date 2026-07
Primary Completion 2027-07 (estimated)
Study Completion 2027-08 (estimated)
Updated on ClinicalTrials.gov 2026-07-07