Clinical Trials Logo

Placenta Accreta clinical trials

View clinical trials related to Placenta Accreta.

Filter by:

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: NCT02784886 Active, not recruiting - Placenta Accreta Clinical Trials

Cell-free Fetal DNA Circulating in the Maternal Plasma as a Marker for Morbidly Adherent Placenta

DNA-Accreta
Start date: November 2013
Phase: N/A
Study type: Observational

The purpose of this study is to determine whether, in a high risk population (placenta praevia and previous caesarean or prenatal suspicion of morbidly adherent placenta (MAP)), the concentration of cell-free fetal DNA circulating in the maternal plasma is significantly increased in the subgroup of morbidly adherent placenta (MAP) cases , in order to determine if the dosage of cell-free fetal DNA circulating in the maternal plasma may be a useful biological tool to detect MAP, alone or in addition to the imagery findings (ultrasonography and RMI).

NCT ID: NCT02729974 Enrolling by invitation - Placenta Accreta Clinical Trials

Use of ROTEM Intraoperatively in Women With Placenta Accreta

ROTEM
Start date: March 2016
Phase: N/A
Study type: Interventional

This study evaluates the use of rapid tests for hematocrit and clotting function in women undergoing surgery for placenta accreta. Half of participants will have these rapid tests performed during surgery to guide blood product transfusion and the other half will have standard lab tests performed to guide transfusion.

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.

NCT ID: NCT02702024 Completed - Placenta Percreta Clinical Trials

The Effectiveness of Double Incision Technique in Uterus Preserving Surgery for Placenta Percreta

Start date: January 2014
Phase: N/A
Study type: Interventional

Placenta percreta is a life-threatening condition that patients are under risk of massive bleeding. It readily necessitates very complicated surgery even leads to mortality. Cesarean hysterectomy is the procedure that is acknowledged worldwide, however, recent studies discussing conservative treatment with segmental resections were published. Fetal extraction and segmental resection could be performed from same (single uterine incision) or two different (double uterine incision) incisions. In this study, the investigators aimed to evaluate the effectiveness and the results of double uterine incision.

NCT ID: NCT02635412 Withdrawn - Placenta Accreta Clinical Trials

Delivery Timing in Morbidly Adherent Placentas: a Randomized, Controlled Trial

MAP
Start date: March 2016
Phase: N/A
Study type: Interventional

This is a randomized controlled trial to investigate the optimal timing of delivery in clinically stable women with a suspected morbidly adherent placenta.

NCT ID: NCT02606474 Not yet recruiting - Clinical trials for Placenta Accreta in Placenta Previa Anterior

Placenta Accreta&Its Complications in Placenta Previa Cases

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

Cases of previous cesarean with placenta previa anterior underwent cesarean section. Placenta accreta is diagnosed during cesarean section &confirmed by pathology. All complications are monitored in cases with placenta accreta and without.

NCT ID: NCT02442518 Recruiting - Placenta Accreta Clinical Trials

Antenatal Diagnosis of Placental Attachment Disorders

ADoPAD
Start date: February 2015
Phase: N/A
Study type: Observational

The accuracy of sonographic prenatal detection of invasive placentation is unclear. The objective of this prospective, multicenter, observational study is to assess the performance of ultrasound for prenatal identification of invasive placentation in women with placenta previa. This study involves more than 25 hospitals in Italy.