Pain Management After Cesarean Delivery and Breastfeeding Initiation
Analgesia
Agnosia+7
+ Behavior
+ Breast Feeding
Prevention Study
Summary
Study start date: January 1, 2024
Actual date on which the first participant was enrolled.This study is dedicated to understanding how different pain management methods after a planned cesarean section affect the start and exclusivity of breastfeeding. The research focuses on women undergoing elective cesarean deliveries with spinal anesthesia, a common situation where pain relief methods can vary. The goal is to see if certain pain management techniques, like TAP blocks or epidural analgesia, improve the likelihood of mothers starting breastfeeding within the first hour after birth and maintaining exclusive breastfeeding for the first 72 hours. This is important as early and exclusive breastfeeding has significant health benefits for both mother and child. Participants in the study will be randomly assigned to receive one of the pain management methods: TAP blocks, epidural analgesia, intravenous multimodal analgesia, or a placebo. These methods are being tested to see which is most effective in reducing post-surgery pain and supporting breastfeeding efforts. The study will measure how comfortable mothers feel breastfeeding and their confidence levels after the cesarean. Participants need to be between 18-45 years old, scheduled for a cesarean, and able to use IV pain control systems. The study is conducted safely with the option for participants to withdraw at any time if they experience any adverse effects.
Protocol
This section provides details of the study plan, including how the study is designed and what the study is measuring.75 patients to be enrolled
Total number of participants that the clinical trial aims to recruit.Prevention Study
Eligibility
Researchers look for people who fit a certain description, called eligibility criteria: person's general health condition or prior treatments.Any sex
Biological sex of participants that are eligible to enroll.From 18 to 45 Years
Range of ages for which participants are eligible to join.Healthy volunteers allowed
If individuals who are healthy and do not have the condition being studied can participate.Conditions
Pathology
Criteria
Study Plan
Find out more about all the medication administered in this study, their detailed description and what they involve.3 intervention groups are designated in this study
This study does not include a placebo group
Treatment Groups
Group I
Active ComparatorGroup II
Active ComparatorGroup III
Active ComparatorStudy Objectives
Primary Objectives
Study Centers
These are the hospitals, clinics, or research facilities where the trial is being conducted. You can find the location closest to you and its status.This study has 1 location