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

RecruitingNAAges 18 Years - 45 YearsFemaleAUSL Romagna Rimini
NCT07202416 on ClinicalTrials.gov ↗
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In plain words

What the trial is, and whether it could suit you

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.

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📋 Eligibility rules (as published)
Inclusion Criteria: * Adult women aged 18-45 years * ASA physical status II-III * Full-term singleton pregnancy scheduled for elective cesarean section under spinal anesthesia Exclusion Criteria: * 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
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What it tests

  • Erector spinae plane block
  • Intrathecal morphine
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Where

1 site
AUSL Romagna - Ospedale M.Bufalini
Cesena, Italy
🤝 Taking part is your choice, and you can leave at any time. Only the trial team can confirm you are eligible — always decide together with your own doctor.
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