About this trial
This study aims to develop a standardized tool to assess intraoperative pain during cesarean delivery under neuroaxial anesthesia. The tool will draw on existing scientific literature, expert clinical opinion and the experiences of patients who have recently undergone caesarean delivery. Experts from multiple disciplines will participate in a structured consensus process (Delphi process) to identify and refine key assessment items. Patient interviews will be conducted to ensure that the tool reflects patient priorities and experiences.
Eligibility criteria
Qualifiers
Signed informed consent
Age > 18 years
Proficient in German or Swiss German
Elective cesarean delivery under neuraxial anesthesia in last 48-72 hours
Disqualifiers
Known fetal abnormalities or neonatal death
Admission of the neonate to the ICU
Severe postpartum hemorrhage of >1000ml blood loss
Preeclampsia
Trial design
Treatments tested in this trial
- Not listed