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Uterine Rupture clinical trials

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NCT ID: NCT04566705 Completed - Mode of Delivery Clinical Trials

Uterine Rupture During Labor Among Women With a Prior Cesarean Delivery

Start date: March 1, 2020
Phase:
Study type: Observational

Although a rare event, uterine rupture during labour is one of the most serious obstetric complications because of the dramatic maternal-fetal consequences that can result. Identifying the risk factors associated with uterine rupture would enable gynecologists to provide patients with risks of uterine rupture in the event of attempted vaginal delivery. The aim of our study is to determine risks factors for uterine rupture during labour in patients with a previous cesarean delivery who have not given birth since and to assess the occurrence of maternal-fetal comply-cations compared to patients with a previous cesarean delivery without uterine rupture.

NCT ID: NCT04449640 Completed - Septum; Uterus Clinical Trials

Uterine Rupture After Hysteroscopic Septum Resection

Start date: July 1, 2020
Phase:
Study type: Observational

To date, several studies have already confirmed a positive effect of hysteroscopic metroplasty on reproductive outcomes in primary infertile women affected by uterine septum, the most common uterine malformation. Nevertheless, very few data are available about the risk of uterine rupture in subsequent pregnancies after hysteroscopic septum resection (HSR). In order to shed about this element, we will retrospectively review the cases of uterine rupture in our setting in the last twenty years, identify which of them had previously undergone HSR, and evaluate the main clinical characteristics for each case.

NCT ID: NCT03052686 Completed - Anomaly Uterus Clinical Trials

Retrospective Study of 110 Cases of Uterine Rupture to Determine Obstetric and Neonatal Complications

RUVO
Start date: January 2000
Phase: N/A
Study type: Observational

This study has for objective to collect medical data from patients with uterine rupture at the childbirth.

NCT ID: NCT02878226 Completed - Maternal Mortality Clinical Trials

Outcomes of Uterine Rupture

Start date: August 2016
Phase:
Study type: Observational

Uterine rupture (UR) is a serious, life-threatening obstetric complication. UR is associated with an increased risk of maternal and perinatal morbidity and mortality, particularly in developing countries compared to developed countries. UR occurs mainly as a consequence of poorly managed labour

NCT ID: NCT00517140 Completed - Pregnancy Clinical Trials

Vaginal Birth After Caesarean Section - Effect on Maternal Psychosocial Function

Start date: September 2003
Phase: N/A
Study type: Interventional

The incidence of caesarean section has reached 15-20% in most developed countries. Encouraging vaginal birth after caesareans section (VBAC) has been considered a key component of a strategy to reduce the caesarean section rate. Most medical literature has focused on the efficacy of VBAC in reducing the caesarean section rate and the physical safety of successful VBAC. However, 30%-40% of these women fail to achieve a vaginal delivery. Little is known about how the uncertainty of labour outcome and a failed VBAC impact on the psychosocial function of these women. We propose to study a cohort of women with a prior caesarean section and presenting with a subsequent pregnancy for care. After consent and recruitment, these subjects will be randomly assigned to have a repeat caesarean section or VBAC. The medical outcomes, overall satisfaction of the subjects with the care they received, and the short-term psychosocial function of these subjects will be studied. The result of this study will provide important information that would be useful in assisting women to decide the mode of delivery after a prior caesarean section.