ESPB vs Intrathecal Morphine for Assessements of Quality of Recovery After Cesarean Section
Trial statusRecruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexFemale
Age18-45
SponsorAUSL Romagna Rimini
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.
Eligibility criteria
Qualifiers
Adult women aged 18-45 years
ASA physical status II-III
Full-term singleton pregnancy scheduled for elective cesarean section under spinal anesthesia
Disqualifiers
ASA ≥ IV
Coagulation disorders
Emergency surgery
Preoperative infection (including infection at the ESPB puncture site)
Trial design
Treatments tested in this trial
- Erector spinae plane block
- Intrathecal morphine
Treatment groups
52 Participants
are divided into 2 treatment groupsSponsors and collaborators
Source ClinicalTrials.gov