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Placenta Accreta clinical trials

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NCT ID: NCT06030492 Recruiting - Placenta Accreta Clinical Trials

Efficacy of Hydrogen Peroxide ( H2O2) in Controlling Placental Site Bleeding in Caesarian Delivery for Placenta Previa / Accreta Spectrum ( PAS)

Start date: January 1, 2023
Phase: N/A
Study type: Interventional

Placenta accreta spectrum (PAS), encompassing the terms placenta accreta, increta, and percreta; abnormally invasive placenta; morbidly adherent placenta; and invasive placentation, is a leading cause of life-threatening obstetric haemorrage (1) . Currently, more than 90% of women diagnosed with PAS also have a placenta praevia (2), and the combination of both conditions leads to high maternal morbidity and mortality due to massive haemorrhage at the time of birth . Maternal mortality of placenta praevia with percreta has been reported to be as high as 7% of cases . Hydrogen peroxide is well-known for its antimicrobial and antiseptic properties. It is used to clean surgical cuts for better localization of bleeding focus in surgery and orthopedics and burn excisions to induce hemostasis . Topical application of hydrogen peroxide was proven to induce hemostasis and reduce operative time in both tonsillectomy and adenoidectomy .

NCT ID: NCT06030479 Recruiting - Placenta Accreta Clinical Trials

Topical Adrenaline Versus Warm Saline Solution for Minimizing Intraperitoneal Bleeding During Caesarian Delivery for Placenta Previa / Accreta Spectrum ( PAS)

Start date: February 1, 2023
Phase: N/A
Study type: Interventional

Placenta accreta spectrum (PAS), encompassing the terms placenta accreta, increta, and percreta; abnormally invasive placenta; morbidly adherent placenta; and invasive placentation, is a leading cause of life-threatening obstetric haemorrage . Currently, more than 90% of women diagnosed with PAS also have a placenta praevia , and the combination of both conditions leads to high maternal morbidity and mortality due to massive haemorrhage at the time of birth . Maternal mortality of placenta praevia with percreta has been reported to be as high as 7% of cases . Adrenaline has also been demonstrated to be a reasonable hemostatic agent because of its low cost, low risk, powerful vasoconstrictor, and platelet aggregation. Topical use of adrenaline is an effective and reasonable hemostatic agent in tonsillectomy.

NCT ID: NCT06029985 Completed - Placenta Accreta Clinical Trials

Hysteroscopic Follow-up Following Conservative Stepwise Surgical Approach for Management of Placenta Previa Accreta

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

Conservative management of placenta accreta spectrum can preserve future fertility but should only be done in hospitals with enough experience as it carries a high risk of maternal complications. Follow up after conservative management is crucial to detect complications early.

NCT ID: NCT06021964 Enrolling by invitation - Clinical trials for Placenta Accreta Spectrum Disorders,Previous Cesarean Section

Prospective Cohort Observational Study of Placenta Accreta Spectrum Disorders

Start date: August 28, 2023
Phase:
Study type: Observational

The incidence of placenta accreta spectrum disorders has shown an increasing trend worldwide due to the increase of cesarean section rate. Research on the outcomes of placenta accreta spectrum disorders primarily relies on retrospective analysis. The aim of this study was to establish a prospective, multicenter cohort in China in order to conduct further investigations on the clinical features, predictive capabilities, diagnostic methods, and pathogenesis of placenta accreta spectrum disorders.

NCT ID: NCT05979181 Completed - Placenta Accreta Clinical Trials

Peripartum Cesarean Hysterectomy for Placenta Percreta

Start date: October 20, 2018
Phase:
Study type: Observational

The aim of this study is to address the possible preoperative determinants of extrauterine diseases in cases of placenta previa percreta and to compare the operative and postoperative characteristics of cases with and without extrauterine disease.

NCT ID: NCT05972915 Not yet recruiting - Accreta, Placenta Clinical Trials

Separation Sign: New Ultrasound Sign to Rule Out Placenta Accreta

Start date: July 30, 2023
Phase:
Study type: Observational

To assess the 'separation sign' as a predictor of normal placental separation in a large cohort of women at risk for placenta accrete spectrum and in a high-risk subgroup with placenta previa or anterior low-lying placenta and have history of at least one previous Cesarean delivery.

NCT ID: NCT05945446 Completed - Clinical trials for Placenta Accreta, Third Trimester

A Serum Galectin-3 Levels in Placenta Accreta Spectrum Pregnancies

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

Placenta Accreta Spectrum (PAS) represents a significant cause of maternal morbidity and mortality, causing complications that surpass those posed by most routine obstetric issues. As such, early detection and proper management of PAS can significantly improve pregnancy outcomes. This study provides an in-depth examination of the serum levels of Galectin-3, a β-galactoside-binding protein, in women experiencing Placenta Accreta Spectrum compared to those with normal pregnancies.

NCT ID: NCT05938062 Completed - Placenta Accreta Clinical Trials

Fibrinogen Concentrate and Placenta Acreta Spectrum

Start date: January 1, 2022
Phase: N/A
Study type: Interventional

The aim of this study is to evaluate the relationship between fibrinogen use and bleeding in patients who underwent cesarean section with a prediagnosis of PAS. The key question(s) it aims to answer are: [Does the use of fibrinogen concentrate reduce bleeding in PAS patients?] Patients who had a cesarean section with a pre-diagnosis of PAS were analyzed retrospectively. The choice of anesthesia applied to the patients and the relationship between the use of blood products and bleeding were evaluated.

NCT ID: NCT05936645 Recruiting - Placenta Accreta Clinical Trials

The Efficacy of a Temporary Sub-Placental Uterine Tourniquet in Minimizing Intraoperative Blood Loss in Management of Placenta Accreta Spectrum Disorder by a Retrograde Cesarean Hysterectomy (Bladder Last)

Start date: August 1, 2023
Phase: N/A
Study type: Interventional

This trial will study the role of a temporary tourniquet around the uterus to reduce blood loss in management of patients with abnormally implanted placenta who will undergo removal of the uterus.

NCT ID: NCT05922397 Recruiting - Placenta Accreta Clinical Trials

Placenta Accreta Spectrum Topographic Classification

Start date: May 21, 2023
Phase:
Study type: Observational

The present study is a prospective multicenter study consisting of a cohort of patients with prenatal or intraoperative diagnosis of PAS, evaluating the clinical outcomes of the group of patients found in each category of the topographic classification. In addition, an approach to evaluate the acceptability of this classification among the obstetrician-gynecologists of the participating medical centers will be included.