About this trial

This prospective observational study aims to assess the impact of epidural analgesia (ELA) on uterine contractility, cardiotocography (CTG) patterns, and maternal-fetal hemodynamics in term pregnancies. The study will recruit 200 laboring patient receiving ELA and evaluate changes in uterine contractions, Doppler blood flow parameters, and fetal heart rate tracings before and after ELA administration. Secondary analyses will compare outcomes between primiparous and multiparous women, as well as between uncomplicated and complicated pregnancies. Pain relief effectiveness will be correlated with observed changes. This study will provide a comprehensive understanding of ELA's effects on labor progression and fetal well-being, addressing gaps in existing research.

Eligibility criteria

Qualifiers

≥ 18 years old

singleton pregnancy

signed informed consent form

patients in labor

Disqualifiers

< than 18 years old

preterm delivery

labor induced or stimulated by oxytocin

multiple pregnancy

Trial design

Treatments tested in this trial

  • Epidural Analgesia

Treatment groups

200 Participants
are divided into 1 treatment group

Locations

1
Clinical Department of Obstetrics and Perinatology at the National Medical Institute of the Ministry of the Interior and Administration02-507, Warsaw Poland

Sponsors and collaborators

Central Clinical Hospital of the Ministry of Internal Affairs and Administration, Warsaw, Poland

Lead sponsor