ESPB vs Intrathecal Morphine for Assessements of Quality of Recovery After Cesarean Section

Recruiting now · Not applicable

Conditions studied: Cesarean Section, Post Operative Pain

In brief

Cesarean section is a surgical procedure that involves significant pain, which is managed through a multimodal pharmacological approach.The primary objective of the study is to evaluate the quality of hospitalization after cesarean section using the QRo11 questionnaire in patients treated with a postoperative Erector Spinae Plane Block compared to those treated with intrathecal morphine.

Key facts

Study ID

NCT07202416

Run by

AUSL Romagna Rimini

People needed

52

Starts

2025-06-18

Expected to finish

2026-06-01

Last updated by the study team

2025-10-01

Who can join

Age: 18 and older, up to 45. Sex: female. Healthy volunteers: not accepted.

You may qualify if…

• Adult women aged 18-45 years
• ASA physical status II-III
• Full-term singleton pregnancy scheduled for elective cesarean section under spinal anesthesia

You may not qualify if…

• ASA ≥ IV
• Coagulation disorders
• Emergency surgery
• Preoperative infection (including infection at the ESPB puncture site)
• Any contraindication to neuraxial analgesia
• History of chronic pain
• Use of opioids
• Allergy to local anesthetics
• Hypersensitivity to any drug used in the study
• Inability to understand or use verbal pain assessment scales
• Refusal to participate in the study

Where it is running

• AUSL Romagna - Ospedale M.Bufalini — Cesena, Forlì, Italy (enrolling)

Full record on ClinicalTrials.gov

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