Clinical Trial

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

Recruiting

Summary

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.

Protocol Amendment History 5 changes

notable Enrollment reduced: 15 -> 12 participants 2026-07-25

minor Completion pushed: 2026-08 -> 2026-09 2026-07-25

critical Recruitment opened 2026-04-30

notable Primary completion pushed: 2026-06 -> 2026-07 2026-04-30

minor Completion pushed: 2026-06 -> 2026-08 2026-04-30

Trial Details

NCT Number	NCT07409012
Lead Sponsor	University Hospital, Basel, Switzerland
Conditions	Elective Cesarean Delivery
Enrollment	12 participants
Start Date	2026-05-11
Primary Completion	2026-06-30 (estimated)
Study Completion	2026-09 (estimated)
Updated on ClinicalTrials.gov	2026-07-24