CompletedNot Applicable

Placental Transfusion and Cord Clamping

Argentina400 participantsStarted 2011-08

Plain-language summary

To compare the evolution of the infant's weight before delayed cord clamping (2 minutes after birth) as an indirect measure of the volume of placental transfusion in a group of healthy and fullterm newborns, placed at the level of the introitus versus another group placed on the abdomen of the mother.

Who can participate

Age range2 Minutes

SexALL

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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: * Term newborns * vigorous born by vaginal delivery * informed consent Signed. Exclusion Criteria: * History of Placenta previa, * postpartum hemorrhage background, * Multiple gestation. * Background of IUGR prenatally diagnosed. * Major congenital malformations diagnosed previous to delivery. * Maternal diseases such as: eclampsia, Rh incompatibility, congestive cardiac failure. * Extraction of blood sample for bank of umbilical cord stem cells. Elimination criteria: * Need for immediate assistance of the newborn, * Birth weight less than 2500 g, * Nuchal cord wrapped too tight, * Major congenital malformations not diagnosed during prenatal period, * Delivery surgically finished Short umbilical cord which might prevent placing the infant in the assigned place .

What they're measuring

Compare infant's birth weight before delayed cord clamping as an indirect measure of the volume of placental transfusion in a group of healthy fullterm newborns placed at the level of the introitus versus at the the mother's abdomen.

Timeframe: inmediately after birth until 2 minutes after birth

Trial details

NCT IDNCT01497353

SponsorFundacion para la Salud Materno Infantil

Sponsor typeOTHER

Study typeINTERVENTIONAL

Primary completion2012-08

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