Clinical Trials Logo

Clinical Trial Summary

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.


Clinical Trial Description

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. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT03899597
Study type Interventional
Source Institute for the Care of Mother and Child, Prague, Czech Republic
Contact Ivan Berka, MD
Phone 0042296511807
Email ivan.berka@upmd.eu
Status Not yet recruiting
Phase N/A
Start date January 30, 2024
Completion date December 30, 2025

See also
  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 NCT06292338 - Lung Sonar in Neonatal Respiratory Disorders
Not yet recruiting NCT06372951 - Lung Ultrasound in Neonatal Intensive Care Units
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