TAP Block Versus ESP Block in Patients Undergoing Elective Cesarean Section: a Randomized Controlled Trial

Trial statusRecruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexFemale
Age18-45
SponsorUniversity of Padova

About this trial

This study is comparing two types of pain relief techniques-TAP block and ESP block-for women having an elective cesarean section. Both techniques involve injecting local anesthetic under ultrasound guidance to numb nerves and reduce pain after surgery. The TAP block mainly relieves pain in the abdominal wall, while the ESP block may reduce both abdominal wall and deeper, organ-related pain. The main goal is to see if there's a difference in pain at rest six hours after surgery. The study will also look at pain at later time points, the amount of opioid medication needed, how quickly women can walk, and when they start breastfeeding.

A total of 156 women will be randomly assigned to receive one of the two blocks after standard spinal anesthesia. Pain will be measured using a simple 0-10 scale at 6, 12, and 24 hours, both at rest and during movement. The study follows strict ethical rules, ensures patient privacy, and all results-whether positive or negative-will be shared to help improve pain management after cesarean delivery.

Eligibility criteria

Qualifiers

Age between 18 and 45 years

Elective cesarean section

Ability to provide informed consent

Disqualifiers

Allergy to any of the drugs used in the study

Heart disease with impaired cardiac function

Stage III or higher kidney failure

Coagulation disorders (platelets <100,000/μL or INR >1.5) or severe liver disease

Trial design

Treatments tested in this trial

  • TAP block
  • ESP block

Treatment groups

90 Participants
are divided into 2 treatment groups

Sponsors and collaborators