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Placenta Previa clinical trials

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NCT ID: NCT04518163 Recruiting - Placenta Previa Clinical Trials

Bakri Balloon Plus Tranexamic Acid During Cesarean Delivery for Placenta Previa

Start date: September 1, 2020
Phase: N/A
Study type: Interventional

Objective to investigate the effect of adjunctive intravenous tranexamic acid (TA) on blood loss during cesarean section (CS) in patients with placenta previa undergone Bakri balloon tamponade

NCT ID: NCT04518150 Recruiting - Placenta Previa Clinical Trials

Combined Bilateral Uterine Artery Ligation and Bakri Balloon During Cesarean Section

Start date: September 1, 2020
Phase: N/A
Study type: Interventional

This study will be performed to compare the effectiveness of routine Bakri balloon tamponade and Bilateral Uterine Artery Ligation during cesarean section in patients with placenta previa

NCT ID: NCT04350645 Recruiting - Clinical trials for Hemorrhage From Placenta Previa, With Delivery

Role of Prophylactic Tranexamic Acid in Reducing Blood Loss During Elective Caesarean Section for Placenta Praevia Major

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

Prophylactic tranexamic acid will reduce blood loss during Caesarean section for placenta praevia

NCT ID: NCT04304625 Recruiting - Clinical trials for Postpartum Hemorrhage

TRAnexamic Acid for Preventing Blood Loss Following a Cesarean Delivery in Women With Placenta pREVIA

TRAAPrevia
Start date: August 7, 2020
Phase: Phase 3
Study type: Interventional

Several randomized, controlled trials, mostly involving women undergoing cesarean delivery, have shown that the prophylactic intravenous administration of 1 g of tranexamic acid after childbirth reduced blood loss. Most were small, single-centre trials with considerable methodologic limitations. It is important to emphasize that none of these RCTs has included women at increased risk of PPH such as placenta previa, a context in which the prevalence of moderate and severe blood loss is significantly higher and where the magnitude of the effect of TXA may highly differ compared to low risk women

NCT ID: NCT04274062 Completed - Nursing Role Clinical Trials

Effects of Peri Partum Integrated Nursing Care Versus Routine Care in Placenta Previa : A Randomized Controlled Trail

Start date: May 1, 2019
Phase:
Study type: Observational

At our institution, the annual number of placenta previa was 494 cases (1.7%); of whom 95 cases (19.2%) were proved to have a placenta accreta. Perioperatively, they are subjected to regular care of a tertiary university hospital. This study aims to determine the effectiveness of peri partum integrated nursing care for the patients with placenta previa versus routine care.

NCT ID: NCT04264234 Completed - Placenta Previa Clinical Trials

Management Of Placenta Previa Cases And Determination Of Hospitalization Criteria

Start date: November 13, 2018
Phase: N/A
Study type: Interventional

Placenta previa cases are one of the difficult groups of patients to manage in modern obstetrics. When the literature is evaluated extensively, no clear information can be seen especially in terms of hospitalization time. Inpatient follow-up of this patients has negative effects like hospital infections in terms of the patient, workload in terms of health personnel and financial losses in terms of the country's economy. Placenta previa cases are complicated patients in which generalizations cannot be easily performed and they should be monitored at third level hospitals. In addition, care should be personalized considering the many reasons. In this study, placenta previa cases will be followed up at 28th gestational week and evaluated at 32nd week by vaginal ultrasonography and MRI and this follow-up will continue until delivery. Thus, in this study, it was aimed to determine the parameters that would allow systematic personalization of health service in this particular patient group by making risk assessment of placenta previa cases.

NCT ID: NCT04215484 Completed - Placenta Accreta Clinical Trials

Placenta Accreta New Detection Procedure by Rapid Assessment of Serum BNP

PANDORA
Start date: January 2, 2020
Phase:
Study type: Observational [Patient Registry]

The placenta accreta is defined as a placenta that is abnormally adherent to the myometrium. It can thus invade the entire thickness of the myometrium (placenta increta) or even exceed the serosa and invade neighboring organs (placenta percreta). It is a rare obstetric pathology with significant morbidity, and its management most often requires hemostatic hysterectomy. Its frequency has increased significantly in recent decades due to the increased rate of caesareans. The maternity center of Tunis ( CMNT ) is a level 3 maternity center, supporting over 12 000 births yearly, where the caesarean section's rate is very high, close to 45% of deliveries. Recently we noted an increase in abnormal placental invasion incidence : in 2018, we report over 60 cases of placenta accreta,increta and percreta. Early detection of these patients can help reduce potential risks. Ultrasound and MRI are the main diagnostic tools, but each one has weaknesses. Biological approch of this diagnosis is not well studied. Recently, BNP has been shown to be associated with increased angiogenesis. Because placenta accreta is characterized by abnormal uteroplacental neovascularization, it has been hypothesized that serum BNP levels may be related to abnormal invasion of the placenta. In the literature, only one study investigated the relationship between cardiac biomarkers (Pro-BNP, CK, CK-MB and troponins) and abnormalities of placental adhesion. The main conclusion was that the Pro-BNP could predict placental accretisation. Thus, the BNP as a mean of screening, could enrich our diagnostic arsenal. The purpose of our study is to determine whether or not BNP can predict abnormal placental invasion during pregnany.

NCT ID: NCT04213755 Completed - Placenta Accreta Clinical Trials

ROTEM in Patients With Placenta Previa

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

The rotational thromboelastogram (ROTEM) test can be performed on patients with placenta previa/accreta/increta/percreta who have a high likelihood of massive bleeding, and the predictors can be identified by comparing the patients who actually show massive bleeding with those who do not. Applying these predictive factors to pregnant women undergoing cesarean section after diagnosis of placenta previa/accreta/increta/percreta, it will be advantageous for the perioperative management because it is possible to select pregnant women with a factor of massive bleeding.

NCT ID: NCT04055194 Recruiting - Placenta Previa Clinical Trials

Antenatal Tranexamic Acid in Women With Symptomatic Placenta Previa

Start date: August 1, 2019
Phase: Phase 2/Phase 3
Study type: Interventional

200 pregnant women with symptomatic placenta previa with previous bleeding attacks attending Ain Shams University maternity hospital will be recruited and randomized to receive either tranexamic acid tablets (500mg four times daily) or placebo. Amount of bleeding during antepartum bleeding attacks will be estimated (by hemoglobin change from baseline at admission till delivery).

NCT ID: NCT03779451 Recruiting - Placenta Previa Clinical Trials

Vaginal Progesterone Versus 17-Alpha-Hydroxyprogesterone Caproate in Placenta Previa

Start date: January 1, 2019
Phase: N/A
Study type: Interventional

Purpose to evaluate the effects of Vaginal Progesterone versus 17-Alpha-Hydroxyprogesterone Caproate for prevention of Emergent Cesarean Delivery in Asymptomatic Pregnant Women with Placenta Previa