Placenta Accreta

11

Review clinical trials related to Placenta Accreta. Use filters to narrow results by trial status, phase, treatment, biological sex and sponsor.

Condition / disease
Location
Status: Not yet recruiting

Evaluation of Cervical Invasion and Length in Placenta Accreta Patients

Placenta accreta spectrum (PAS), also called morbidly adherent placenta, is a serious pregnancy problem where the placenta attaches too deeply to the uterus wall and does not come out normally after birth. This often happens after previous cesarean sections or when the placenta is low (placenta previa). It can cause heavy bleeding, serious complications, and danger to the mother. This study will look at pregnant women with PAS at Sohag University Hospital in Egypt. Researchers will use ultrasound to check two things: How much the placenta has invaded the cervix (the lower part of the uterus). The length of the cervix. The main goals are to find out: How common cervical invasion is in PAS cases. What happens to women who have this invasion (outcomes like bleeding or surgery needs). If a short cervix is linked to early labor (preterm birth). Women with confirmed PAS will join this observational study from March 2026 to January 2028. They will have extra ultrasound scans during pregnancy. No new treatments or drugs are tested - the study only collects information from routine care and scans to better understand the condition. This research may help doctors predict risks earlier, plan safer deliveries, and improve care for mothers and babies with PAS in the future.

Participants needed: 200
Trial details
Biological sex: FemaleType: ObservationalSponsor: Sohag UniversityUpdated: Mar 5, 2026Duration: 16 Weeks
Eligibility criteria

Pregnant women aged 18-45 years with suspected or confirmed PAS based on prenata... [+3]

Multiple gestation. [+1]

Status: Recruiting

Evaluation of Clinical Outcomes and Acceptability of an Anatomical Classification for Placenta Accreta Spectrum

This study evaluates the clinical implementation of intra-operative topographic classification system for PAS. In addition to a standard of care risk stratification prenatal ultrasound for patients with a risk of PAS, this study adds an additional intraoperative surgical staging protocol to validate the classification system, improve surgical approach, and significantly clinical outcomes of pregnant people with an a prior risk of PAS. The study will involve pregnant patients with PAS risk factor, include data collection spanning prenatal assessment, intraoperative classification, surgical technique implementation and postoperative analysis. The anticipated study duration is approximately 36-48 months.

Participants needed: 60
Trial details
Age: 18-55Biological sex: FemaleType: ObservationalSponsor: University of California, Los AngelesUpdated: Jan 16, 2026Locations: 1
Eligibility criteria

Pregnant people suspected of having PAS based on ultrasound findings or clinical... [+5]

Patients who decline participation or withdraw consent [+1]

Status: Not yet recruiting

A Comparison Between Bladder Dissection Before and After Uterine Incision During Cesarean Section for Placenta Accreta Spectrum: A Randomized Controlled Study

The worldwide incidence of placenta accreta spectrum is increasing, following the trend of rising caesarean delivery. It is an heterogeneous condition associated with a high maternal morbidity and mortality rate (Jauniaux et al., 2018). caesarean hysterectomy is considered the gold standard for the treatment of placenta accreta. Also this radical approach is associated with high rates of severe maternal morbidity as hemorrhage and insult to surrounding organs during surgery (Hoffman et al., 2010). Surgeons should be able to dissect the bladder safely and confidently through minimally invasive techniques, to avoid surgical injury, it is important to use anatomic landmarks, minimize the use of cauterization (Farhat and Casale, 2018). All centers are encouraged to develop guidelines to manage the potential urologic complications of these cases tailored to their resources (Taneja and Shah, 2017). This study aims to evaluate the timing of bladder dissection in caesarean section in patient with placenta accreta spectrum.

Participants needed: 80
Trial details
Age: 18-45Biological sex: FemaleType: InterventionalSponsor: Ain Shams UniversityUpdated: May 4, 2025
Eligibility criteria

Women with BMI at or under 35kg/m2 [+5]

o History of urinary bladder injury. [+3]

Status: Recruiting

Diagnosis and Outcomes of Placental Accretism

The goal of this observational study is to evaluate the diagnostic ability of the main criteria currently adopted for the diagnosis of placenta accreta and to define the maternal outcomes in terms of complications of the different management strategies currently adoptable when placental accretism is suspected.

Participants needed: 70
Trial details
Age: 18-44Biological sex: FemaleType: ObservationalSponsor: IRCCS Azienda Ospedaliero-Universitaria di BolognaUpdated: Feb 19, 2025Locations: 7
Eligibility criteria

Age between 18 years and 44 years [+2]

Status: Recruiting

Placenta Accreta Spectrum Topographic Classification

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.

Participants needed: 326
Trial details
Age: 18-55Biological sex: FemaleType: ObservationalSponsor: Fundacion Clinica Valle del LiliUpdated: Feb 13, 2025Locations: 1
Eligibility criteria

Pregnant woman over 18 years old. [+3]

None.

Status: Recruiting

3D Placental Volume in Placenta Accreta

Placenta Accreta spectrum is a major obstetric disease nowadays. Different methods are used for antenatal diagnosis. In our study, investigators are aiming to compare 2 common ways for diagnosis, i.e; 3D Ultrasound and 2D with color Doppler.

Participants needed: 38
Trial details
Biological sex: FemaleType: ObservationalSponsor: Assiut UniversityUpdated: Jan 1, 2025Locations: 1
Eligibility criteria

pregnant women with placenta previa

congenital anomalies of placenta Placental separation Uterine anomalies

Status: Not yet recruiting

The Placental Thickness and Pregnancy Outcomes in Placenta Previa Women

Placenta previa is the placenta overlying the cervical os. Placenta previa is about 1 in 200 pregnancies. The risk factors are the increasing rate of cesarean section and previous uterine surgery. Placenta previa is associated with many adverse complications; the most serious one is related to maternal hemorrhage. The diagnosis of placenta previa is done by trans-abdominal and trans-vaginal ultrasonography, which can document the placental edge's relationship to the internal os. Placenta accreta spectrum disorder is defined when trophoblastic invades the myometrium. The Placenta accreta spectrum can be categorized as: placenta accreta, placenta increta, and placenta percreta. The clinical utility of placental thickness is an area of ongoing research in placenta previa. Prior studies have demonstrated an association between mid-trimester placental thickness and placenta accreta spectrum. Despite the presence of many studies in characterizing placental thickness, most studies have focused primarily on the placental accreta spectrum lacking information about other fetal and maternal complications. Symptomatic (bleeding) placenta previa is associated with increased maternal and neonatal morbidity and mortality. In addition; the mechanism that involves bleeding is unclear. It is usually related to uterine contractions, cervical effacement, and dilation leading to separation of the placenta from the underlying decidua.

Participants needed: 140
Trial details
Age: 20-35Biological sex: FemaleType: InterventionalSponsor: Assiut UniversityUpdated: Dec 5, 2024Locations: 1
Eligibility criteria

Pregnant women from 32-34 weeks. [+5]

Women with severe bleeding necessitate immediate delivery. [+3]

Status: Not yet recruiting

Evaluation of Planned Conservative Surgical Management of Placenta Accreta Spectrum in Women's Health Center, Assiut University Hospital

In recent years, with the application of an abdominal artery balloon and the improvement of surgical techniques, efforts are made to preserve the uterus for patients PAS. the aim of the study To evaluate conservative surgical management of placenta accreta spectrum in Assiut University hospital regarding maternal and fetal outcomes.

Participants needed: 150
Trial details
Age: 18+Biological sex: FemaleType: ObservationalSponsor: Assiut UniversityUpdated: Dec 2, 2024
Eligibility criteria

Pregnant women with history of previous caesarean section. [+4]

Gestational age less 28 weeks. [+5]

Status: Not yet recruiting

Tamponade vs Partial Myometrial Resection of Lower Uterine Segment in Management of Placenta Accreta Spectrum Cases

To compare the efficacy of lower uterine tamponade and partial lower myometrial resection in the management of intraoperative bleeding in cases with placenta accreta spectrum .

Participants needed: 222
Trial details
Biological sex: FemaleType: InterventionalSponsor: Assiut UniversityUpdated: Aug 28, 2024
Eligibility criteria

1-Pregnant women with placenta previa /PAS diagnosed before delivery (by ultraso...

A pre-existing decision of performing intrapartum hysterectomy

Status: Recruiting

Simplified Conservative Measures in Managing Morbidly Adherent Placenta in Beni-Suef University

To evaluate the efficacy of modified uterine artery ligation and myometrial compression as a conservative measure in improving the prognosis of the morbidly adherent placenta.

Participants needed: 172
Trial details
Age: 25-45Biological sex: FemaleType: InterventionalSponsor: Nesreen Abdel Fattah Abdullah ShehataUpdated: Jun 20, 2024Locations: 1
Eligibility criteria

Gestational age more than 28 weeks as determined by LMP and ultrasound. [+4]

Vaginal bleeding [+1]

Status: Recruiting

Single-step Placenta Accreta Resective Technique Tourniqueted vs Absence, Conservative Uterine Surgery

Background: An optimal international standard for PAS surgery is not yet available, and the establishment of a suitable surgical method is an important focus of in PAS management. Objective: To assess the efficacy and safety of tourniquet uses for conservative approach in the management of placenta accerta spectrum. Patients and Methods: 40 pregnant women who underwent conservative management of placenta accrete at Kasr El-Aini hospital (Obstetrics and gynecology department - Faculty of medicine - Cairo university) were included and were divided according to the use of tourniquet into 2 equal groups: Study group (tourniquet group): consists of 20 women for whom tourniquet was used in the lower part of the uterus during surgical treatment of placenta accreta spectrum.Control group (no tourniquet group): consists of 20 women for whom no tourniquet was used.

Participants needed: 40
Trial details
Age: 20-40Biological sex: FemaleType: InterventionalSponsor: Cairo UniversityUpdated: Jun 4, 2024Locations: 1
Eligibility criteria

Pregnant females with previous CS deliveries (at least 1). [+3]

Maternal age above 40 years. [+3]