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Postpartum Hemorrhage clinical trials

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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: NCT02277067 Recruiting - Clinical trials for Postpartum Hemorrhage

Carbetocin Versus Misoprostol in High Risk Patients for Postpartum Hemorrhage After C.S.

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

We will compare between Carbitocin and Misoprostol in prevention of postpartum hemorrhage in high risk patients after C.S.

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: NCT02187874 Recruiting - Clinical trials for Postpartum Haemorrhage

Timing of Umbilical Cord Occlusion in Premature Babies( <33 w). Delayed vs Early.

CODE-P
Start date: July 2014
Phase: N/A
Study type: Interventional

Early cord clamping after delivery has been common practice for many decades as part of the active management of the third stage of labour. However in recent years, several studies have shown that delayed cord clamping may offer important benefits to the newborn. The data gathered indicate that delayed cord clamping may be particularly useful in premature babies, between 26 and 32 weeks of gestational age, reducing the need for blood transfusion and the incidence of intraventricular haemorrhage. However it is argued that the described potential benefits of delayed cord clamping could be negated by the increased risk of polycythaemia and jaundice in the newborn, as well as by potential interference with the postpartum haemorrhage management, initial care and reanimation of the premature newborn, and the possibility of cord blood donation. These factors, together with as the lack of homogeneity among existing studies regarding the delayed cord clamping technique create the need, in our opinion, for further research, to establish the proper place of this measure. Our hypothesis is that delayed cord clamping in the premature newborn significatively reduces the need for blood transfusions and intraventricular haemorrhage, compared with usual early cord clamping. Secondary outcomes: - To define the impact of delayed cord clamping on neonatal assessment parameters after delivery: APGAR score, cord pH, need for mechanical ventilation or reanimation. - Neonatal mortality and morbidity - Effect of the procedure on the incidence and severity of maternal postpartum haemorrhage - To study the correlation between Iron metabolism and reticulocitary haemoglobin levels in cord and infant blood.

NCT ID: NCT02136719 Recruiting - Clinical trials for Postpartum Haemorrhage

Bimanual Uterine Compression to Reduce Blood Loss and Prevent Postpartum Haemorrhage After Vaginal Delivery

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

the investigators aim to compare bimanual uterine compression immediately after delivery of the placenta for 5 minutes versus no intervention for the prevention of postpartum hemorrhage in Women at high risk for primary atonic postpartum hemorrhage. The primary outcome is postpartum haemorrhage (blood loss of ≥ 500 ml) while the Secondary outcomes include use of additional uterotonics and need for blood transfusion.

NCT ID: NCT02080104 Recruiting - Clinical trials for Postpartum Hemorrhage

Intramuscular Versus Intravenous Prophylactic Oxytocin for Hemorrhage After Vaginal Delivery

oxytocin
Start date: February 2014
Phase: N/A
Study type: Interventional

Intramuscular versus intravenous prophylactic oxytocin for the third stage of labour following vaginal delivery: A randomised controlled trial

NCT ID: NCT01932060 Recruiting - Clinical trials for Postpartum Hemorrhage

Oxytocin Infusions and Blood Loss in Patients Undergoing Elective Cesarean Delivery.

Start date: August 2013
Phase: Phase 3
Study type: Interventional

Although prior dose-finding studies have investigated the optimal bolus dose of oxytocin to initiate adequate uterine tone, it is unclear what oxytocin infusion regimen is required to maintain adequate uterine tone after delivery. The study investigators aim to compare two different infusion rates of oxytocin to assess the optimal infusion regimen for reducing blood loss in women undergoing elective Cesarean delivery.

NCT ID: NCT01600612 Recruiting - Clinical trials for Postpartum Hemorrhage

Oxytocin, Carbetocin and Misopristol for Treatment of Postpartum Hemorrhage: A Multicentric Randomized Trial

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

Postpartum hemorrhage (PPH) is the leading cause of maternal death worldwide, with an estimated mortality of 140 000 per year. Uterine atony is one of the most important causes of PPH. The traditional treatment of which is the use of uterotonic agents. Oxytocin is the most conventional drug which was proved effective. However, it has the shortcomings of short half life and the necessity of intravenous administration. Misopristol, and more recently Carbetocin were introduced for treatment of atonic PPP not responding to Oxytocin. Aim of the study is to evaluate the effectiveness of Carbetocin, Misopristol, and Oxytocin for treatment of atonic PPH.

NCT ID: NCT01579201 Recruiting - Clinical trials for Postpartum Hemorrhage

ED90 Determination of Carbetocin for the Prevention of Uterine Atony in Women Undergoing an Elective Cesarean Delivery

Start date: March 2012
Phase: Phase 4
Study type: Interventional

The purpose of this trial is to determine the effective dose of carbetocin which would prevent the occurrence of postpartum uterine atony in 90% of women undergoing an elective cesarean delivery.

NCT ID: NCT01382732 Recruiting - Clinical trials for Postpartum Hemorrhage

Carbetocin vs. Oxytocin for Prevention of Postpartum Bleeding in Patients With Severe Preeclampsia

Start date: January 2012
Phase: Phase 3
Study type: Interventional

Postpartum hemorrhage is an important cause of maternal morbidity and mortality. In patients with severe preeclampsia there is an increased risk of postpartum hemorrhage but the hemodynamic changes associated with this pathology make the management of any kind of bleeding particularly troublesome. There are many pharmacological options, being oxytocin the first line of treatment. However there is no evidence about the safety and efficacy of carbetocin, an oxytocin agonist. The investigators aimed to compare oxytocin with carbetocin for the routine prevention of postpartum hemorrhage in patients with severe preeclampsia.