Actively Recruiting
Development of a Patient-Centered Assessment Tool for Pain During Cesarean Delivery
Led by University Hospital, Basel, Switzerland · Updated on 2026-04-29
15
Participants Needed
1
Research Sites
13 weeks
Total Duration
On this page
AI-Summary
What this Trial Is About
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.
CONDITIONS
Official Title
Development of a Patient-Centered Assessment Tool for Pain During Cesarean Delivery
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Signed informed consent
- Age > 18 years
- Proficient in German or Swiss German
- Elective cesarean delivery under neuraxial anesthesia in last 48-72 hours
- Delivery of a healthy infant of at least 35+1 weeks of gestation
You will not qualify if you...
- Known fetal abnormalities or neonatal death
- Admission of the neonate to the ICU
- Severe postpartum hemorrhage of >1000ml blood loss
- Preeclampsia
- Current psychiatric disease, e.g. schizophrenia, personality disorders
- Substance abuse
- Chronic pain disease
AI-Screening
AI-Powered Screening
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Trial Site Locations
Total: 1 location
1
University Hospital Basel
Basel, Canton of Basel-City, Switzerland
Actively Recruiting
Research Team
L
Lena Gschwandtner
CONTACT
How is the study designed?
Study Type
OBSERVATIONAL
Masking
N/A
Allocation
N/A
Model
N/A
Primary Purpose
N/A
Number of Arms
0
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