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Evaluation of Breastfeeding Success and Self-Efficacy in Mothers Giving Birth Via Vaginal Delivery or Cesarean Section

Breastfeeding Clinical Trial

Official title:
Evaluation of Breastfeeding Success and Self-Efficacy Using LATCH in Mothers Giving Birth Via Vaginal Delivery or Cesarean Section: Cross-sectional Study

Clinical Trial Summary

This cross-sectional observational study was conducted to compare breastfeeding success and breastfeeding self-efficacy levels of mothers who gave birth via vaginal delivery (spontaneous or via epidural analgesia) or cesarean section (under general or spinal anesthesia).

Clinical Trial Description

This study was conducted by including women, who gave birth via VD or CS in the gynecology clinics of a training and research hospital and a city hospital and were in the postpartum period (after 24 hours). It compared the breastfeeding self-efficacy and breastfeeding success of mothers who gave birth via CS (under spinal anesthesia or general anesthesia) with those of mothers who gave birth via vaginal delivery (under epidural analgesia or via spontaneous vaginal delivery). ;

Study Design

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT05106634
Study type Observational [Patient Registry]
Source Aydin Adnan Menderes University
Contact
Status Completed
Phase
Start date September 10, 2019
Completion date October 22, 2021
View Details
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