SuspendedNot Applicable

Maternal Outcomes Following Manual Lysis of the Placenta.

Stopped: Insufficient resources.

Israel100 participantsStarted 2018-11-20

Plain-language 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 maternal satisfaction, time to first breastfeeding, length of hospital stay, infection rate etc.

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: * 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.

What they're measuring

Hemoglobin Drop

Timeframe: within 24 hours after delivery

Trial details

NCT IDNCT03626844

SponsorHaEmek Medical Center, Israel

Sponsor typeOTHER

Study typeINTERVENTIONAL

Primary completion2020-09

View on ClinicalTrials.gov More Third Stage of Delivery trials