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Placenta Previa clinical trials

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NCT ID: NCT03266432 Recruiting - DIC Syndrome Clinical Trials

Thromboelastometry Guided DIC Prevention After Cesarean Section in Pregnant Women With Placenta Previa

DIC
Start date: August 28, 2017
Phase: N/A
Study type: Interventional

Evaluation of the use of thromboelastometry for early identification of the underlying coagulopathy and to guide individualized transfusion therapy to prevent DIC development during ICU stay after cesarean section in women with placenta previa who require a massive blood transfusion.

NCT ID: NCT03124472 Recruiting - Placenta Previa Clinical Trials

Effect of Uterine Artery Ligation Prior to Uterine Incision in Women With Placenta Previa

Start date: June 1, 2017
Phase: N/A
Study type: Interventional

Pfannenstiel incision of skin and opening of the anterior abdominal wall in layers. - The loose peritoneum of the lower uterine segment is dissected downwards to mobilize the urinary bladder and expose the lower uterine segment. - Uterine artery ligation was performed by grasping the broad ligament with thumb anterior and the index finger lifting the base below the site uterine incision; the uterine artery was singly ligated with No. 1 vicryl suture. Myometrium was included so that uterine vessels are not damaged. - Cresenteric lower uterine segment incision was performed as usual. Higher incisions were performed in cases where the traditional incision was expected to be directly through the placenta Delivery of the baby and placenta. - Closure of the uterine incision in 2 layers with N0. 1 vicryl suture. - Closure of the anterior abdominal wall in layers

NCT ID: NCT02590484 Recruiting - Placenta Previa Clinical Trials

The Cervix as a Natural Tamponade in Postpartum Hemorrhage Caused by Placenta Previa and Placenta Previa Accreta

Start date: June 2012
Phase: N/A
Study type: Interventional

Placenta previa and placenta accrete carry significant maternal and fetal morbidity and mortality. Several techniques have been described in the literature for controlling massive bleeding associated with placenta previa cesarean sections. The aim of this study is to evaluate the efficacy and safety of the use of the cervix as a natural tamponade in controlling postpartum hemorrhage caused by placenta previa and placenta previa accreta.

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.

NCT ID: NCT02303418 Recruiting - Clinical trials for Post Partum Haemorrhage

Carbetocin Versus Oxytocin in the Prevention of Post Partum Haemorrhage (PPH) in Women Undergoing Caesarean Sections for Placenta Previa: A Randomised Controlled Trial

Start date: November 2014
Phase: Phase 3
Study type: Interventional

The study aims at comparing the roles of carbetocin and oxytocin in the prevention of atonic PPH in women undergoing CS for placenta previa. 200 women will be randomly divided into 2 equal groups using computer generated random numbers, Group 1 will receive Carbetocin 100 µgm (Pabal® Ferring, UK) and group 2 will receive oxytocin 5IU (Syntocinon®, Novartis, Switzerland).

NCT ID: NCT02277041 Recruiting - Clinical trials for Postpartum Hemorrhage

Carbetocin Versus Misoprostol in Cases With Placenta Previa After C.S.

PPH
Start date: October 2014
Phase: Phase 4
Study type: Interventional

We will compare efficacy and safety of Carbetocin with Misoprostol in prevention of postpartum hemorrhage in Placenta previa women after C.S.

NCT ID: NCT02270593 Recruiting - Placenta Previa Clinical Trials

ADAMTS,Proteoglycan and Oxidant / Antioxidant Enzyme Levels of Placenta Previa Totalis (Accreta, Increta, Percreta).

Start date: August 2013
Phase: N/A
Study type: Observational [Patient Registry]

Placenta previa totalis (accreta, increta, percreta); ADAMTS and proteoglycans and the oxidant / antioxidant enzyme levels.