Epidural Anesthesia in Labor and Delivery

2

Review clinical trials related to Epidural Anesthesia in Labor and Delivery. Use filters to narrow results by trial status, phase, treatment, biological sex and sponsor.

Condition / disease
Location
Status: Not yet recruiting

The Effects of Epidural Analgesia on Maternal-Infant Bonding and Birth-Related Trauma

This prospective, single-center study aims to evaluate the effects of epidural analgesia on maternal-infant bonding and perceived birth-related trauma in women undergoing vaginal delivery. Participants will be divided into two groups: those who receive epidural analgesia and those who deliver without it. Standardized questionnaires will be used to assess pain perception, maternal satisfaction, and the quality of early bonding between mother and infant. The study is designed in accordance with the Declaration of Helsinki and Good Clinical Practice guidelines, with approval from the local ethics committee.

Participants needed: 80
Trial details
Age: 18+Biological sex: FemaleType: InterventionalSponsor: Adiyaman University Research HospitalUpdated: Jul 22, 2025Locations: 1
Eligibility criteria

Not listed

Status: Not yet recruiting

EPidural's Impact on Contractions and Fetal REsponse

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.

Participants needed: 200
Trial details
Age: 18+Biological sex: FemaleType: ObservationalSponsor: Central Clinical Hospital of the Ministry of Internal Affairs and Administration, Warsaw, PolandUpdated: Mar 6, 2025Locations: 1
Eligibility criteria

≥ 18 years old [+6]

< than 18 years old [+8]