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Clinical Trial Summary

Postpartum hemorrhage is the leading cause of maternal deaths in all over the world, especially in developing and underdeveloped countries. Medical and surgical methods exist for management of bleeding. There are two surgical techniques for removal of the placenta on cesarean delivery, which are called manual removal and controlled cord traction. In manual removal group, the duration of surgery time might be shorter theoretically. Nevertheless, there are studies showing that manual removal of the placenta may increase postpartum endometritis and postpartum hemorrhage. The optimal method for removal of the placenta during the cesarean delivery remains uncertain (1). It is a known fact that uterine massage after vaginal birth lowers the risk of postpartum hemorrhage (2) However, there is no study on how effective uterine massage is during cesarean delivery. In 2018, Saccone and colleagues wanted to publish a meta-analysis on the role of uterine massage in reducing postpartum bleeding during cesarean delivery, but when they examined the literature on the subject, they could not find a study which included only the group that gave birth by cesarean section and was free from bias. In the same publication, it was mentioned that it was necessary to investigate the effectiveness of uterine massage, which is a cost-free method that can reduce maternal morbidity in underdeveloped countries where maternal deaths due to postpartum bleeding are high, in cesarean section. (3)


Clinical Trial Description

In this study, data of patients who underwent emergency cesarean delivery in the Department of Obstetrics and Gynecology, Ankara Etlik City Hospital, will be collected The parameters to be examined in the research are as follows: 1. Patients' postoperative 30th minute, 1st and 2nd hour systolic blood pressure, diastolic blood pressure, pulse rate, shock indexes 2. Volume of diuresis at postoperative first six hours 3. Hemoglobin and hematocrit values at preoperatively and 2nd, 6th, 24th hours postoperatively. 4. Duration of the surgery. 5. Need for additional dose of uterotonics 6. Need for surgical methods to manage postpartum bleeding 7. Duration of hospital stay The sample size of this study was calculated with the Gpower3.1 computer program. The total number of samples with 90% power and 95% confidence interval was calculated as 338 patients. The number of volunteers to participate in our study is planned to be 360 in total, 60 volunteers for each group, across 6 groups. Results will be considered statistically significant for p< 0,05. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT06192836
Study type Observational
Source Ankara Etlik City Hospital
Contact sumeyye saritas
Phone +903122790000
Email etliksh.iletisim@saglik.gov.tr
Status Not yet recruiting
Phase
Start date January 10, 2024
Completion date February 22, 2025

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