ESPB vs Intrathecal Morphine for Assessements of Quality of Recovery After Cesarean Section
Recruiting
N/A
Interventional Study
Cesarean Section
Post Operative Pain
No Placebo Group
Every participant receives an active treatment — no one gets a placebo.
At a Glance
- Age
- 18 – 45
- Sex
- Female
- Study type
- Interventional
- Purpose
- Treatment
- Participants needed
- 52 (estimated)
- Sponsor
- AUSL Romagna Rimini · Other
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About This Trial
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.
Trial Locations
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Eligibility Criteria
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 …
Contacts