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Placenta Accreta clinical trials

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NCT ID: NCT03707132 Completed - Placenta Accreta Clinical Trials

Tourniquet Reduces Blood Loss in Postpartum Hemorrhage During Hysterectomy for Placenta Accreta

Start date: October 1, 2014
Phase:
Study type: Observational

Monocentric prospective observational study comparing the use of tourniquet in low uterus segement versus standard procedure in hysterectomy owing to placenta accreta

NCT ID: NCT03668795 Completed - Clinical trials for To Publish Our Experience in the Surgical Management to Placenta Accreta Cases and the Maternal Outcome

Surgical Management of Placenta Accreta

Start date: August 1, 2011
Phase:
Study type: Observational

purpose of this study was to report our experience for surgical management of suspected placenta accreta cases encountered in King Hussein medical center

NCT ID: NCT03570710 Completed - Clinical trials for Cesarean Section Complications

Reducing Blood Loss During Cesarean Hysterectomy for Placenta Accreta Spectrum

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

PAS is an obstetrics condition that is closely linked with massive obstetrical hemorrhage with a varied incidence about once in every 533 live births. It is considered one of the causes of massive transfusion (>4 units of packed red blood cells) and cesarean hysterectomy. It is estimated that peripartum hysterectomies are performed in approximately0.08% of all deliveries. A large study from the United Kingdom noted that 38% were a result of PAS. More recently, population-based analyses show that PAS is the indication for the majority of peripartum hysterectomies. Bleeding at the time of peripartum hysterectomy for PAS is often substantial. Nearly 90% of patients need blood products, while 38% of patients need a massive blood transfusion. There is a 30% risk of an ICU admission, thromboembolic disease, readmission, reoperation, poor wound healing, and a reported rate of surgical re-exploration ranging from 4% to 33%. The risk of maternal death reported being as high as 7% (although less in most recent series) Therefore, adequate homeostatic techniques are essential. Currently, surgical hemostasis can be secured by a variety of methods, including mechanical sutures (or clamping), electric coagulation, ultrasonically activated scalpel or drugs. TA is a lysine analog which acts as an antifibrinolytic via competitive inhibition of the binding of plasmin and plasminogen to fibrin. The rationale for its use in the reduction of blood loss depending on the implication of the coagulation and fibrinolysis processes . However, concerns about possible thromboembolic events with the parental administration of TA has stimulated increasing interest in its topical Use

NCT ID: NCT03327818 Completed - Placenta Accreta Clinical Trials

Comparison Between Hysterectomy and Conservative Management in Treatment of Placenta Accreta Regarding Maternal Complication

Start date: June 2016
Phase: N/A
Study type: Observational

AIM OF THE WORK The aim of the study is to compare the maternal morbidity and mortality between obstetric hysterectomy and conservative surgery for pregnant ladies > 28 weeks with placenta accreta during caesarean section at Ain Shams University Maternity Hospital in the last five years and prospective study in the next six months. Hypothesis In women with placenta accrete undergoing hysterectomy may be similar to conservative surgery as regard maternal morbidity and mortality.

NCT ID: NCT03032770 Completed - Placenta Accreta Clinical Trials

Early Prediction of Placenta Accreta by Ultrasound and Color Doppler

Start date: January 1, 2017
Phase:
Study type: Observational

Placenta accreta is a substantially life threatening condition and one of the causes of maternal morbidity and mortality in the world. According to study done in United Kingdom, The estimated incidence of placenta accreta/increta/percreta was 1.7 per 10,000 maternities overall and 577 per 10,000 in women with both a previous cesarean delivery and placenta previa. in a tertiary south Italian center, The incidence increased from 0.12% during the 1970s, to 0.31% during the 2000s.While in United States of America, the prevalence of placenta accreta was 3.7 per 1000 deliveries.

NCT ID: NCT02966197 Completed - Placenta Accreta Clinical Trials

Efficacy of Prophylactic Internal Iliac Artery Balloon Catheterization in the Management of Placenta Previa and Accreta

Start date: June 2015
Phase: N/A
Study type: Interventional

Placenta previa and accreta both could potentially cause serious postpartum hemorrhage and even maternal death. Interventional radiological techniques have been developed to limit massive hemorrhage during caesarean section. This study investigated the efficacy of prophylactic internal iliac artery balloon catheterization in management for placenta previa and accreta.

NCT ID: NCT02943421 Completed - Clinical trials for Decrease Maternal Morbidity

Transverse B-Lynch in Management of Placenta Accreta

Start date: December 1, 2016
Phase:
Study type: Observational

Placenta accreta is considered a severe pregnancy complication that may be associated with massive and potentially life-threatening intrapartum and postpartum hemorrhage. Life-threatening bleeding is the most common complication to be associated with this condition; the average blood loss at time of delivery is reported to be 3000-5500 mL, which leads to significant postoperative morbidity and death.

NCT ID: NCT02806024 Completed - Cesarean Section Clinical Trials

Perioperative Administration of Tranexamic Acid for Placenta Previa and Accreta Study

TAPPAS
Start date: November 2016
Phase: Phase 4
Study type: Interventional

The purpose of this pilot study is to determine if intravenous tranexamic acid (TXA) is effective for reducing blood loss during high risk surgical procedures related to placenta previa and placenta accreta. TXA is currently used in other types of surgery for patients who are expected to have a large blood loss, such as orthopedic or open heart surgery.

NCT ID: NCT02728232 Completed - Placenta Percreta Clinical Trials

Internal Iliac Artery Ligation and Abnormally Invasive Placenta

Start date: April 2016
Phase: N/A
Study type: Interventional

This trial is set to detect the impact of bilateral internal iliac artery ligation on the amount of intra-operative blood loss during the hysterectomy procedure done for the management of abnormally invasive placenta

NCT ID: NCT02712099 Completed - Placenta Accreta Clinical Trials

TUI 3D in Diagnosis of Placenta Accreta: Comparison With Gray-scale and Color Doppler Techniques

Start date: August 2015
Phase: N/A
Study type: Observational

The purpose of this study is to evaluate the potential of the 3 D TUI view in diagnosis of morbidly adherent placenta in comparison to 2D grayscale, color Doppler and intraoperative findings.