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Placenta Accreta clinical trials

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NCT ID: NCT05542043 Completed - Clinical trials for Postpartum Hemorrhage (PPH)

Risk Factors for Postpartum Hemorrhage in Patients With Histologically Verified Placenta Accreta

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

This retrospective, monocentric study aims to examine risk factors for postpartum hemorrhage in women with histologically verified placenta accreta. Women with histologically verified placenta accreta are divided into two groups: women with normal blood loss (BV < 500 ml) versus women with increased blood loss (BV ≥ 500 ml). The clinical data of pregnant women with histologically verified placental disorders, who gave birth in the Women's Clinic University Hospital Basel (USB) between 1986 and 2019, are compared with each other.

NCT ID: NCT05500404 Completed - Clinical trials for Placenta Accreta Spectrum

Diagnostic Accuracy of Placental Thickness in Lower Uterine Segment Measured By Ultrasound in Prediction of Placenta Accreta Spectrum in Patients With Placenta Previa. A Diagnostic Test Accuracy Study

Start date: December 1, 2021
Phase:
Study type: Observational

Current prenatal diagnosis of placenta accrete spectrum disorders relies on subjective individual interpretations of visual sonographic findings on grayscale and color Doppler imaging. When blinded to clinical data, there is significant interobserver variability in the diagnosis of invasive placentation. This study will evaluate placental thickness among pregnant women with placenta previa and determine if increased placenta thickness correlates with the risk for placenta accreta spectrum (PAS) disorders.

NCT ID: NCT05419804 Completed - Placenta Accreta Clinical Trials

Placenta Accreta; Total Lower Uterine Segmentectomy With Cervico-corporeal Anastomosis

Start date: June 1, 2022
Phase:
Study type: Observational

To study feasibility and safety of Total lower uterine segmentectomy with cervico-corporeal anastomosis in conservative management of placenta accreta

NCT ID: NCT05013749 Completed - Placenta Accreta Clinical Trials

Histerectomy Vs Partial Myometrial Resection for Placenta Accreta Spectrum

RCT-PAS
Start date: August 20, 2021
Phase: N/A
Study type: Interventional

Currently, Placenta Accreta Spectrum (PAS) has two treatment options: hysterectomy (completely removing the uterus) and partial myometrial resection (resecting the part of the uterus affected by this pathology). The present study is a feasibility study of a multicenter, randomized controlled clinical trial to be carried out in 3 health institutions. Patients who meet the inclusion criteria, after signing the informed consent, will be taken to the surgical procedure and before the start of the procedure they will be randomized to one of the two interventions, hysterectomy or partial myometrial resection, intra-surgical clinical outcomes will be explored and a follow-up will be carried out during the immediate post-surgical period (72 hours), in 7 to 12 days and at 42 days postpartum. A sample size of 60 patients is estimated among the 3 health institutions, with an approximate duration of the study of 24 months.

NCT ID: NCT04981483 Completed - Placenta Accreta Clinical Trials

Conservative Surgery for Placenta Accreta

Start date: January 1, 2018
Phase: N/A
Study type: Interventional

A stepwise surgical approach for conservative management of placenta previa accreta.

NCT ID: NCT04911322 Completed - Placenta Accreta Clinical Trials

Pulmonary Artery Doppler and Neonatal Outcome in Placenta Accreta Spectrum Patients

Start date: August 15, 2021
Phase:
Study type: Observational

To correlate ultrasonographic markers of fetal lung maturity including Pulmonary artery Doppler indices in the late preterm and early term in placenta accreta spectrum patients with neonatal outcome.

NCT ID: NCT04689516 Completed - Pulmonary Edema Clinical Trials

Thoracic Fluid Content During Hypervolemic Hemodilution

Start date: December 24, 2020
Phase: N/A
Study type: Interventional

Thoracic fluid content (TFC) is one of the many variables measured by the ICON electrical cardiometry (EC) device (Osypka Medical). The ICON device is often called "thoracic electrical bio-impedance" that based on measuring the changes in total resistance of the thorax to electric current and is considered a numerical measure of total (intravascular and extravascular) thoracic fluid. Although TFC is a measure of both extra and intra-vascular thoracic fluid, it provides an estimate of the increase in intrathoracic fluids such as to facilitate the risk of pulmonary edema. Although many studies were done on the ability of TFC to detect pulmonary edema in preeclampsia, ARDS, heart failure, weaning from mechanical ventilation and during fluid management in prolonged surgery , yet, there is no study before was done on the use of TFC as a guide for fluid therapy during hypervolemic hemodilution in major obstetric surgery in patients with placenta accreta as one of the most common etiologies of life-threatening obstetric hemorrhage and the most common cause of peripartum hysterectomy Aim of the work: To use TFC as a guide for 6% HES infusion of hypervolemic hemodilution in patients with placenta accreta to avoid fluid overload. Objectives: - To calculate LUS score at the end of infusion. - To evaluate TFC in k ohm-1. - To assess oxygen saturation, PO2 and P/F ratio in ABG. - To calculate the total infused volume in milliliters.

NCT ID: NCT04683562 Completed - Placenta Accreta Clinical Trials

Netrin-1 and Placenta Accreta

Start date: December 1, 2021
Phase: N/A
Study type: Interventional

Netrin-1 is a secreted protein, which was first identified as a neuronal guidance factor. It is expressed in a multitude of tissues as pancreas, lung, breast, and placenta. Netrin-1 is a multifunctional protein, involved in cell polarity, adhesion, angiogenesis, apoptosis, migration, morphogenesis, and differentiation of various cell types. Most of netrin-1 activity occur through signaling pathways induced by its two main receptors, DCC (deleted in colorectal cancer) and UNC5H (uncoordinated-5 homolog). Its receptors have been linked to the processes of apoptosis and angiogenesis. In absence of netrin-1, DCC and UNC5H receptors lead to apoptosis. In contrary, in presence of netrin-1, receptors transduce molecular cascades leading to proliferation, differentiation and migration of the cells. Netrin-1 has been involved in the pathogenesis of multiple diseases, as diabetes, cardiovascular diseases, and cancer. Serum Netrin-1 levels were high in preeclamptic patients.

NCT ID: NCT04660578 Completed - Placenta Accreta Clinical Trials

A.Chohan Continuous Squeezing Suture (ACCSS) for Placenta Previa / Accreta

ACCSS
Start date: February 12, 2019
Phase: N/A
Study type: Interventional

Placenta praevia and accreta spectrum disorders are rising in incidence due to increased rate of repeat caesarean sections. Peripartum hysterectomy remains the only definitive treatment of massive postpartum haemorrhage related to this condition. A multitude of conservative treatments is described in literature, which includes pelvic devascularization under radiological control, myometrial resection with placenta in situ, and various suturing techniques some involving inversion of cervix. Variable success rates are described, but search continues for a simple, safe and effective treatment. Such a surgical technique i.e. A. Chohan Continuous Squeezing Suture (ACCSS) is described in this study for controlling haemorrhage from the lower uterine segment at caesarean section for placenta praevia and accrete spectrum disorders.

NCT ID: NCT04628169 Completed - Clinical trials for Pathophysiology of Placenta Accreta

Impact of Netrin-1 in the Pathophysiology of Placenta Accreta Spectrum

Start date: December 1, 2021
Phase:
Study type: Observational

The main goal of this study the possible involvement of netrin-1 into the pathophysiology of placenta accrete spectrum. To delineate the role of netrin-1, neogenin - zeb1 signaling pathway in mechanism of morbidly adherent placenta.