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Assessment of the efficacy of using intraumbilical vein injection of oxytocin after delivery of newborn in reducing postpartum hemorrhage

Not Applicable
Conditions
postpartum hemorrhage.
Third-stage haemorrhage
Registration Number
IRCT201204179491N1
Lead Sponsor
Qazvin University of Medical Sciences
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Complete
Sex
Female
Target Recruitment
200
Inclusion Criteria

Inclusion criteria : vaginal delivery;gestational age 37-42 weeks;singleton pregnancy;live fetus;cephalic presentation;neonatal birth weight 2500-4500 gram;parity 1-3.
exclusion criteria : blood pressure140/90 or greater;placenta previa;placental abruption;abnormal placentation;instrumental delivery;history of postpartum hemorrhage;
history of curretage or cesarean delivery or any uterine scar;coagulopathy;hydramnios;known uterine anomaly;large episiotomy or vaginal lacerations those were repaired in operation room.

Exclusion Criteria

Not provided

Study & Design

Study Type
interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Assessment of the efficacy of using intraumbilical vein injection of oxytocin in active management of the third stage of labor in reducing postpartum hemorrhage. Timepoint: 24 hours after intervention. Method of measurement: hemoglobin level(gr/dl).
Secondary Outcome Measures
NameTimeMethod
Incidence of retained placenta need for manual removal of placenta in each group. Timepoint: in third stage of labor. Method of measurement: percentage.;Incidence of using additional uterotonics in each group. Timepoint: during the third stage of labor and 24 hours later. Method of measurement: percentage.;Incidence of falling hemoglobin levels in each group. Timepoint: during the third stage of labor and 24 hours later. Method of measurement: gr/dl.;Duration of the third stage of labor in each group. Timepoint: during the third stage of labor. Method of measurement: minutes and seconds.;Incidence of transfusion after delivery in each group. Timepoint: during 24 hours after delivery. Method of measurement: percentage.
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