13 results
Aim of the study is to get informed on the outcome of women treated in the MUMC for obstetric anal sphincter injury between 2005 and 2012. The controlgroup is matched for maternal age at delivery, parity, mode of delivery and child weigth.
To assess if the *BasIQ* makes a standardized incision of 4 cm.
To judge if there is a difference between referral rates during labour when an amniotomy is performed in the latent phase of labour, compared to an expectant policy.
To study the validity of the AN24 monitor for uEMG monitoring of uterine contractions compared to intra-uterine pressure monitoring during labour.
The objective of this study is to find out is the way contractions are maesurent during labor are of any influence on the lenght and the way women deliver. It also looks if there is any influence on neonatal outcome.
To objective the most efficacy way to ripening the cervix of pregnant women.
The aim of this study is to test the hypothesis that severe pre-eclampsia/HELLP syndrome in comparison to patients without severe preeclampsia/HELLP are accompanied by changes in hepatic circulation and themselves cause changes in elastographic…
Primary objective: To identify those groups of pregnant patients, planned to undergo cesarean delivery, who are at risk to develop severe hypotension (defined as a decrease of at least15% from the baseline tension) based on their preoperative volume…
The main aim of this study is to improve knowledge on the hemodynamic burden of labour in women with cardiac disease and women without cardiac disease, by examining CO trajectory through the full course of labour. Therefore, we specified the…
To develop a prediction model for women with one previous caesarean section by combining assessment of the lower uterine segment with an extensive antepartum history taking and postpartum follow up.
Primary objective is assessment of the pharmacokinetic profile of MPD in pregnancy. Secondary objectives are the safety and efficacy of any use of MPD during pregnancy.
Primary objectives: The main objective of this Post Market Clinical Follow-Up (PMCF) study is to further evaluate and monitor the safety and performance of the *BasIQ-4®* in a population of women delivering in general hospitals in The Netherlands…
In women with early, mild PPH (blood loss 500-750ml) we would like to establish whether restrictive resuscitation strategy reduces the progression to severe PPH (blood loss > 1000 ml) compared to care as usual