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UnknownNCT02136719

Bimanual Uterine Compression to Reduce Blood Loss and Prevent Postpartum Haemorrhage After Vaginal Delivery

Status
Unknown
Phase
N/A
Study type
Interventional
Enrollment
520 (estimated)
Sponsor
Benha University · Academic / Other
Sex
Female
Age
19 Years – 49 Years
Healthy volunteers
Not accepted

Summary

the investigators aim to compare bimanual uterine compression immediately after delivery of the placenta for 5 minutes versus no intervention for the prevention of postpartum hemorrhage in Women at high risk for primary atonic postpartum hemorrhage. The primary outcome is postpartum haemorrhage (blood loss of ≥ 500 ml) while the Secondary outcomes include use of additional uterotonics and need for blood transfusion.

Detailed description

the investigators conduct a prospective non- randomized study at Department of Obstetrics and Gynecology, Benha University Hospital, since April 2014 till May 2016, after approval of the study protocol by the Local Ethical Committee. A written informed consent is obtained from eligible women before induction or at early stage of labour. Women with singleton pregnancies of more than 28 weeks' gestation who are admitted to hospital and candidates for vaginal delivery are eligible for the study .Gestational age more than 28 weeks the gestational age is determined based upon the date of the first day of last normal menstrual period and confirmed by ultrasound scan during the 1st trimester. The patients (520) are divided into two groups, Group A (260) receive bimanual uterine compression immediately after delivery of the placenta for 5 minutes while Group B (260) receive no intervention. The third stage of labour was managed as usual by clamping and cutting of umbilical cord, waiting for signs of placental separation and delivering the placenta by controlled cord traction. Duration of the 3rd stage of labour is calculated. Patients are kept in labor room under observation for a period of 1 h. Measurement of blood loss by a clean plastic lined absorbent drape placed under the woman's buttocks to collect all the blood lost after delivery of the baby and drainage of the amniotic fluid. The drape is changed as many times as needed. The woman stays on the drape or asked to wear a pad over the next 60 minutes. In the case of severe haemorrhage, the investigators follow the usual guidelines for management of postpartum haemorrhage, and the supplemental treatment registered. All drapes and pads are weighed on an electronic scale and the known dry weight of the linen is subtracted. As 1 ml of blood weighs close to 1 g, the balance in grams is assumed to be the total blood loss in ml.

Conditions

Interventions

TypeNameDescription
PROCEDUREbimanual uterine compressionbimanual uterine compression immediately after delivery of placenta for 5 minutes

Timeline

Start date
2014-04-01
Primary completion
2020-12-01
Completion
2020-12-01
First posted
2014-05-13
Last updated
2020-03-10

Locations

1 site across 1 country: Egypt

Source: ClinicalTrials.gov record NCT02136719. Inclusion in this directory is not an endorsement.