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Placenta Previa clinical trials

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NCT ID: NCT03779438 Recruiting - Placenta Previa Clinical Trials

17-Alpha-Hydroxyprogesterone Caproate in Pregnant Women With Placenta Previa

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

Purpose to evaluate the effects of intramuscular 17-Alpha-Hydroxyprogesterone Caproate (17-OHPC) for prevention of Emergent Cesarean Delivery in symptomatic Pregnant Women with Placenta Previa

NCT ID: NCT03774667 Recruiting - Placenta Previa Clinical Trials

Characteristics, Complications and Perinatal Outcomes in Placenta Previa Women

Start date: January 1, 2019
Phase:
Study type: Observational [Patient Registry]

This study aim to investigate the characteristics, complications and perinatal outcomes in pregnant women with placenta previa.

NCT ID: NCT03772184 Completed - Placenta Previa Clinical Trials

Modified Cervical Inversion During CS in Placenta Previa

Start date: January 10, 2019
Phase: N/A
Study type: Interventional

There is an increasing rates of placenta previa nowadays

NCT ID: NCT03741114 Recruiting - Placenta Previa Clinical Trials

Foley's Catheter Balloon Plus Tranexamic Acid During Cesarean Delivery for Placenta Previa

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

Placenta previa (PP) is an obstetric condition that is closely linked with massive obstetric hemorrhage with a varied incidence about once in every 150-250 live births. Insertion of intrauterine balloon tamponade has been suggested in the management of massive postpartum hemorrhage (PPH). The Bakri balloon has a sausage-like spindle shape and a drainage lumen and is made of silicon. It has been used in cases of uterine atony and placenta previa with a success rate of 90%. However, Bakri balloon is not available in all countries. The aim of this study is to evaluate the efficacy of the use of intrauterine inflated Foley's catheter balloon with or without intravenous tranexamic acid to control PPH during cesarean delivery in cases of placenta previa.

NCT ID: NCT03741075 Recruiting - Clinical trials for Cesarean Section Complications

Topical Tranexamic Acid Plus Bilateral Uterine Artery Ligation During Cesarean Delivery

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

Placenta previa (PP) is an obstetric condition that is closely linked with massive obstetric hemorrhage with a varied incidence about once in every 200 live births. It is considered one of the causes of the increased need for blood transfusion and cesarean hysterectomy. PPH due to PP typically starts during cesarean section (CS) in the placental bed, at the lower uterine segment mostly after placental separation. Proceeding for cesarean hysterectomy can be the only effective line of management in spite of the associated high morbidity rate. Various conservative measures have been developed to avoid hysterectomy and preserve fertility in patients with PP. Bilateral Uterine artery ligation (BUAL) is one of the reported surgical procedures carried out in these cases as it is easy and quick. It can be used alone or with adjunctive measures with a fair success rate. The aim is to reduce the blood supply to the uterus and to prevent postpartum hemorrhage. Tranexamic acid 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 implicated in the control of PPH. However, concerns about possible thromboembolic events with parenteral administration of TA have stimulated increasing interest in its topical use.

NCT ID: NCT03725553 Completed - Placenta Previa Clinical Trials

Intra-myometrial Vasopressin During Cesarean Section in Placenta Previa

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

Placenta previa can have serious adverse consequences for the mother, including an increased risk of maternal mobility, antenatal and intrapartum hemorrhage, and the mother may, therefore, require a blood transfusion or even an emergency hysterectomy. Although it is a relatively rare condition with an overall incidence of 0.28-2.0% of all deliveries, it has been suggested that the incidence of placenta previa is increasing. Many gynecological surgeons use a local injection of vasopressin, which is a known peripheral vasoconstrictor, at the time of laparoscopic myomectomy to decrease blood loss. In addition, the useful role for local infiltration of vasopressin to arrest hemorrhage from the placental bed has been demonstrated in several obstetrical case reports. The vasopressin V1α receptor has been demonstrated to be present in the myometrium of both non-pregnant and pregnant women and contributes to myometrial contraction. Therefore, the investigators evaluated the effect of local injection of vasopressin on the blood loss and secondary impact on complications during cesarean section in cases of placenta previa.

NCT ID: NCT03682510 Recruiting - Clinical trials for Cesarean Section Complications

B-Lynch Transverse Compression Suture Versus a Sandwich Technique (N&H Technique) for Complete Placenta Previa

Start date: October 31, 2018
Phase: N/A
Study type: Interventional

Obstetric hemorrhage is estimated to be responsible for about 30% of all maternal deaths and is the leading direct etiology of maternal mortality worldwide . Especially in developing countries, hemorrhage is by far the leading cause of mortality and morbidity, with 140,000 women dying of PPH worldwide each year, which equates to 1 death every 4 min . The United Nations Millennium Development Fifth Goal, to reduce 75 % of maternal mortality by 2015 that not reached yet, cannot be held without significant improvements in postpartum hemorrhage (PPH) related mortality. Placenta previa (PP) is an obstetric condition that is closely linked with potentially life-threatening hemorrhage with varied incidence approximately four or five per 1000 pregnancies. Placenta previa is diagnosed when the placenta obstructs part or all the cervical os during antenatal ultrasonography. Placenta previa may be subclassified using ultrasound scan to be "major or complete" (implanted across the cervix) or "minor" (not implanted across the cervix). Currently, there is a dramatic increase in the incidence of placenta previa due to the increasing rate of cesarean delivery combined with increasing maternal age (6) It is considered one of the causes of the increased need for blood transfusion and cesarean hysterectomy. Various conservative measures have been developed to avoid hysterectomy and preserve fertility in patients with PP. Bilateral Uterine artery ligation (BUAL) is one of the reported surgical procedures carried out in these cases as it is easy and quick. It can be used alone or with adjunctive measures with a fair success rate. The aim is to reduce the blood supply to the uterus and to prevent PPH. There are a few methods to prevent and treat placenta previa bleeding immediately after cesarean delivery and control intra-operative bleeding during the cesarean operation. A safe intra-operative maneuver to arrest bleeding due to placenta previa is required. However, there is no gold standard treatment of placenta previa hemorrhage. The aims of the study to assess the effect of the novel sandwich technique for the control of hemorrhage during cesarean section due to placenta previa (double Transverse Compression Suture at the lower uterine segment plus Intrauterine inflated Foley's Catheter Balloon, (N&H technique) on control of massive bleeding due to central placenta previa in comparison with B-Lynch Transverse Compression Suture.

NCT ID: NCT03638024 Recruiting - Placenta Accreta Clinical Trials

Cell-free Fetal DNA Concentration in Cases of Abnormal Placental Invasion .

Start date: September 1, 2018
Phase:
Study type: Observational

Cell free fetal DNA might predict abnormal placental invasion

NCT ID: NCT03633175 Recruiting - Placenta Previa Clinical Trials

Progesterone in Patients With Placenta Previa

Start date: July 5, 2018
Phase: Phase 2
Study type: Interventional

This study evaluates the efficacy of prophylactic vaginal progesterone administration in reducing of the episodes of antepartum hemorrhage and subsequent prevention of preterm delivery in women with placenta previa.

NCT ID: NCT03570723 Completed - Clinical trials for Post Partum Hemorrhage

Glove-loaded Foley's Catheter Tamponade for Cesarean Section for Placenta Previa

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

Objective: To investigate the effect of A glove-loaded Foley's catheter tamponade versus stepwise uterine devascularization on blood loss during cesarean section (CS) in patients with complete placenta previa.