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Obstetric Labor Complications clinical trials

View clinical trials related to Obstetric Labor Complications.

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NCT ID: NCT02853058 Recruiting - Labor Complication Clinical Trials

Uterine Artery Pulsatility Index and Materno Fetal Outcomes

UADLAB
Start date: July 2016
Phase: N/A
Study type: Interventional

High Uterine artery index pulsatility (PI) is associated with small for gestationnal age but also with stillbirth and distress during labor.

NCT ID: NCT02834897 Completed - Clinical trials for Pregnancy Complications

Performance Evaluation of System EOS Imaging in Pelvimetry Versus Pelvi-scanner

PELVI-EOS
Start date: May 2015
Phase: N/A
Study type: Interventional

The purpose of this study and demonstrate the reliability of EOS imaging system in the measurement of internal diameters of obstetrical pelvis versus "Goldstandard current "that is the pelviscanner.

NCT ID: NCT02804555 Completed - Clinical trials for Obstetrical Complication of Anesthesia

Effects of Intraoperative Oxygen Therapy on Oxygenation of Newborns Born Via Elective Cesarian Section

Start date: June 2013
Phase: N/A
Study type: Interventional

In this study the investigators examine the effects of intraoperative oxygen administration to the mother on certain enzyme functions of the newborn. With this object blood samples are taken from the newborn's umbilical chord - which is otherwise a routine practice at the investigators clinic - and the mother's radial artery in parallel with umbilical clamping and cutting for blood gas and reactive oxygen species analyses. Samples are analyzed locally in a properly equipped laboratory.

NCT ID: NCT02759510 Not yet recruiting - Clinical trials for Hemodynamic Instability

Cardiac Output Changes in Cesarean Section

Start date: June 2016
Phase: Phase 0
Study type: Interventional

Since 2011, phenylephrine was recommended as the preferred drug to maintain blood pressure in obstetric anesthesia.Phenylephrine, an α adrenoceptor agonist, can induce peripheral vasoconstriction to maintain blood pressure, while reflexly decrease heart rate and result in cardiac output (CO) reduction.Norepinephrine acts not only as an α adrenoceptor receptor agonist, but also as a weaker β adrenergic receptor agonist. It can elevate blood pressure the same asphenylephrine, meanwhile produce positive inotropic effect including increasing heart rate.Thus, the administration of norepinephrine can maintain blood pressue and avoid the decline of CO. The purpose of this study is to evaluate the effect of norepinephrine and phenylephrine on maternal CO in cesarean section by transesophageal echocardiography.

NCT ID: NCT02614053 Active, not recruiting - Clinical trials for Antepartum Hemorrhage

Plethysmography Variability Index Monitoring for Parturients With Antepartum Hemorrhage

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

The purpose of this study is to evaluate the use of continuous noninvasive intraoperative plethesmography variability index in conjunction with Hemoglobin levels monitoring using Masimo Radical-7™ Pulse CO-Oximeter during elective cesarean sections in patients with antepartum and intrapartum hemorrhage as a guide for fluid and blood transfusion practice .

NCT ID: NCT02542748 Completed - Hypotension Clinical Trials

Comparison of Norepinephrine and Ephedrine on Hypotension After Spinal Anesthesia in Parturients

Start date: October 5, 2015
Phase: N/A
Study type: Interventional

Incidence of hypotension is high in parturients after spinal anesthesia. Ephedrine could be used to treat hypotension but lead to lower fetal pH as well. This study is to compare the effects of norepinephrine and ephedrine on hypotension in parturients.

NCT ID: NCT02461251 Completed - Hemorrhage Clinical Trials

Thromboelastometry-guided Treatment Protocol Versus Standard Care of Major Haemorrhage in Obstetric Patients

ROTEM-PPH
Start date: January 2016
Phase: N/A
Study type: Interventional

This is a prospective, randomized and controlled study to find out if a rotational thromboelastometry(ROTEM) guided treatment protocol reduces the need for blood transfusions in major obstetric haemorrhage compared to standard care of clinical decision making, conventional coagulation tests and massive transfusion protocol. Secondary aim is to find out if ROTEM can predict the incidence of thromboembolic events in this patient group.

NCT ID: NCT02447757 Completed - Clinical trials for Complication of Labor and/or Delivery

Efficacy and Satisfaction With Remifentanil Analgesia in Parturients During the Childbirth

Start date: January 2010
Phase: N/A
Study type: Observational

Retrospective observational study to determine the efficacy of remifentanil during the delivery. Authors will search the data in period between 2010 and 2014 in cohort of 100 parturients and obtain data of analgesic efficacy (VAS score after remifentanil analgesia induction) and parturients satisfaction with the method.

NCT ID: NCT02427854 Completed - Clinical trials for Complication of Labor and Delivery

Palestinian Perineum and Birth Complication Study

PPS
Start date: February 2015
Phase: N/A
Study type: Interventional

In this study the investigators want to assess complications associated to pregnancy and delivery, and interventions used during labor. Pregnancy and delivery related complications are a major health problem globally. Events during labor such as excessive bleeding, uterine rupture, emergency cesarean delivery; other instrumental deliveries and anesthesia problems are situations that potentially may lead to severe outcomes for the mother and child. Diabetes, anemia and hypertensive disorders may also complicate both the pregnancy and delivery. Between 60-80% of women delivering their first baby need suturing due to perineal tears (tears located to the area between the vagina and anus). Superficial perineal tears rarely cause long-term problems, but often lead to pain and discomfort immediately after birth. Deeper or severe perineal tears, involving the anal sphincter, may influence the woman's quality of life. This is mainly due to long-lasting pain, discomfort and sexual dysfunction, and the fact that obstetric anal sphincter tear is the main cause of anal incontinence. Recent clinical intervention studies have shown that the incidence of severe obstetric perineal tears may be reduced by 50-70% by introducing a bimanual support technique of the perineum. In these studies all midwives and gynecologists were trained in the bimanual support technique. When it comes to training in new medical techniques in general, some studies have shown that use of animated instructions on mobile phones may be a good alternative to the more traditional "hands-on" or "bedside" teaching methods. In a global perspective, it is important to study the efficacy of mobile units for transferring of new knowledge, especially for use in resource constrained settings.

NCT ID: NCT02326077 Suspended - Clinical trials for Obstetric Labor Complications

Sonopartogram. The Next Step in the Delivery Room

SONOLABOR
Start date: October 1, 2020
Phase:
Study type: Observational

Objectives: - Evaluation of the correlation between the sonographic parameter and clinical findings (e.g. digital examination) in any cephalic (not only occipital anterior) position - Examination of the relationship between various sonographic parameters - Determination of intraobserver and interobserver variation in obtaining the sonographic measurements - Analysis of the temporal variation of the different sonographic measurements in normal spontaneous vaginal delivery versus obstructed labor in fetuses with occiput anterior versus those with persistent occiput posterior - Establishment of a sonopartogram that should replace in an objective way Friedmann - Establishment of cut-off values that may help clinicians to choose between vaginal operative delivery or caesarean section - Another interesting aspect of intrapartum transperineal ultrasound imaging is whether there is a psychological benefit to the patient in being able to follow on the ultrasound screen how fetal head descent and position are being assessed objectively.