Neonatal Respiratory Distress Clinical Trial
Official title:
A Prospective, Randomized and Placebo Controlled Trial Comparing the Role of ARTificial Uterine CONtractions and no Intervention in Perinatal Respiratory Morbidity of Term Infants Delivered by Elective Caesarean Section - ARTCON Study
In this study, the investigators aim to investigate if artificial uterine contractions prior to elective caesarean section delivery may have an impact on the respiratory morbidity of term neonates.
Accumulating evidence suggests that the respiratory morbidity of infants is lower if delivered by caesarean section after the spontaneous onset of uterine contractions, or after oxytocin exposure. Moreover, benefits for the mother due to stretching of the lower uterine segment and possible lower blood loss are plausible. In obstetrics, there is a well described and standardized way to induce artificial uterine contractions in order to predict fetal wellbeing and tolerance of labor, without inducing the labor itself. This is the oxytocin challenge test (OCT). Although the OCT has not been performed previously in the context of planned elective caesarean section deliveries, it is generally considered a safe procedure if appropriate monitoring is granted. Hence evaluation of the role of artificial uterine contractions in perinatal respiratory morbidity of term infants delivered by elective caesarean section is possible and of interest. ;
Status | Clinical Trial | Phase | |
---|---|---|---|
Terminated |
NCT05030012 -
Maintaining Optimal HVNI Delivery Using Automatic Titration of Oxygen in Preterm Infants
|
N/A | |
Active, not recruiting |
NCT04780412 -
Efficacy of Misoprostol in Prevention of Neonatal Respiratory Morbidity in Parturient at Early Term Elective Caesarian Section
|
Phase 3 | |
Completed |
NCT05257499 -
In-person Versus Online Debriefing in HBB
|
N/A | |
Terminated |
NCT04096235 -
A Study to Evaluate the Use of the Neotech RAM Nasal Cannula for CPAP and Bi-PAP Application in Infants 28-42 Weeks Gestation in a Neonatal Intensive Care Unit (NICU)
|
N/A | |
Recruiting |
NCT05737095 -
Study of the Feasibility of Early Lung Ultrasound in Neonatal Respiratory Distress in Premature Newborns Born Between 32 Weeks of Amenorrhea and 36 Weeks Plus 6 Days of Amenorrhea, Hospitalized in the Neonatal Pediatrics and Intensive Care Units of the Dijon University Hospital
|
||
Completed |
NCT06171867 -
PNEUMACRIT Device for Neonatal Cardio Respiratory Monitoring
|
N/A | |
Recruiting |
NCT02030691 -
Tolerance of nHFPV Versus nCPAP in Neonatal Respiratory Distress
|
N/A | |
Not yet recruiting |
NCT06372951 -
Lung Ultrasound in Neonatal Intensive Care Units
|
||
Not yet recruiting |
NCT06292338 -
Lung Sonar in Neonatal Respiratory Disorders
|
||
Completed |
NCT06198478 -
Tandem: Skin-to-skin Transfer From the Delivery Room to the Neonatal Unit
|
||
Recruiting |
NCT06356909 -
Study of PREMEdication Before Laryngoscopy in Neonates in France
|
||
Recruiting |
NCT03239327 -
Vaginal Misoprostol to Improve the Neonatal Respiratory Outcome
|
N/A | |
Completed |
NCT04051762 -
A Comparative Study Between Postextubation of Preterm Infants Into High-Flow Nasal Cannulae V.S Nasal Continuous Positive Airway Pressure
|
||
Not yet recruiting |
NCT05144724 -
Volume Targeted Mask Ventilation Versus Pressure Ventilation in Preterm Infants
|
N/A | |
Recruiting |
NCT02978976 -
Effect of Antenatal Steroid on Pulmonary Artery Blood Flow
|
Phase 4 | |
Completed |
NCT06285669 -
Effects of Kinesiotaping on Respiratory Muscles in Very Preterm Infants
|
N/A | |
Recruiting |
NCT06207994 -
PRICO: OPTI Target Range
|
N/A | |
Recruiting |
NCT05274386 -
Evaluation of the Impact of SpO2 Averaging Time on Performance of an Automatic FiO2 Control System: a Randomized Study
|
N/A | |
Recruiting |
NCT02020993 -
Urine NT-ProBNP in Neonatal Respiratory Distress
|
N/A | |
Recruiting |
NCT04947215 -
The Association Between LPCAT1 Genetic Polymorphism and Stress Biomarkers in Neonatal Respiratory Distress Syndrome
|