Completed

Pain Management After Cesarean Delivery and Breastfeeding Initiation

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What is being tested

Analgesia

Procedure
Who is being recruted

Agnosia+7

+ Behavior

+ Breast Feeding

From 18 to 45 Years
+12 Eligibility Criteria
See all eligibility criteria
How is the trial designed

Prevention Study

Interventional
Study Start: January 2024
See protocol details

Summary

Principal SponsorKonya City Hospital
Last updated: January 28, 2026
Sourced from a government-validated database.Claim as a partner

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.

Official TitleThe Effect Of Post-Birth Analgesia Interventions Performed To Purposed Of Elective Cesarean Delivery With Spinal Anesthesia In Our Hospital On The Initiating Of Breastfeeding And Exclusive Breastfeeding.
NCT06682871
Principal SponsorKonya City Hospital
Last updated: January 28, 2026
Sourced from a government-validated database.Claim as a partner

Protocol

This section provides details of the study plan, including how the study is designed and what the study is measuring.
Design Details

75 patients to be enrolled

Total number of participants that the clinical trial aims to recruit.

Prevention Study

Prevention studies aim to stop a disease from developing. They often involve people at risk and test things like vaccines, lifestyle changes, or preventive medications.


Eligibility

Researchers look for people who fit a certain description, called eligibility criteria: person's general health condition or prior treatments.
Conditions
Criteria

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

AgnosiaBehaviorBreast FeedingFeeding BehaviorNervous System DiseasesNeurologic ManifestationsPerceptual DisordersSigns and SymptomsPathological Conditions, Signs and SymptomsNeurobehavioral Manifestations

Criteria

7 inclusion criteria required to participate
Written informed consent;

18-45 years old;

ASA Physical Status 1-3;

Scheduled for elective cesarien delivery;

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5 exclusion criteria prevent from participating
Hepatic disease, e.g. twice the normal levels of liver enzymes;

Kidney disease, e.g. twice the normal level of serum creatinine;

Bupivacaine sensitivity or known allergy;

Anticoagulants considered to be a contraindication for TAP blocks;

Show More Criteria

Study Plan

Find out more about all the medication administered in this study, their detailed description and what they involve.
Treatment Groups
Study Objectives

3 intervention groups are designated in this study

This study does not include a placebo group 

Treatment Groups

Group I

Active Comparator
Infants of mothers who received Epidural analgesia after inactive elective spinal cesarean section (25 patients)

Group II

Active Comparator
Infants of mothers who received Multimodal intravenous analgesia after inactive elective spinal cesarean section (25 patients)

Group III

Active Comparator
Infants of mothers who received 4-Quadrant TAP block after inactive elective spinal cesarean section (25 patients)

Study 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

Suspended

Konya City Hospital

Konya, Turkey (Türkiye)Open Konya City Hospital in Google Maps
CompletedOne Study Center