Development of a Patient-Centered Assessment Tool for Pain During Cesarean Delivery

Trial statusRecruiting
Trial phaseNot listed
Trial typeObservational
Biological sexFemale
Age18+
SponsorUniversity Hospital, Basel, Switzerland

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

Trial groups

No trial groups listed