NCT03899597 - The Role of ARTificial Uterine CONtractions in Perinatal Respiratory Morbidity of Term Infants Delivered by Elective Caesarean Section | Biotech Hunter

Enrollment

200

Participants

Timeline

Start Date

January 30, 2024

Primary Completion Date

September 30, 2025

Study Completion Date

December 30, 2025

Conditions

Neonatal Respiratory Distress

Interventions

DRUG

Oxytocin

The intervention group (ARTCON) will receive the standard assignment for the elective caesarean section, but at least one hour before surgery oxytocin exposure will be performed with cardiotocographic (CTG) monitoring and obstetrical supervision.

OTHER

Normal saline

The control group (SA) will receive the standard assignment for the elective caesarean section, but at least one hour before surgery placebo exposure will be performed with cardiotocographic (CTG) monitoring and obstetrical supervision.

Trial Locations (1)

14700

Institute for the Care of Mother and Child, Prague

All Listed Sponsors

lead

Institute for the Care of Mother and Child, Prague, Czech Republic

OTHER