Development of a Patient-Centered Assessment Tool for Pain During Cesarean Delivery
Recruiting
Observational Study
Elective Cesarean Delivery
Healthy Volunteers Welcome
You do not need to have the condition being studied to take part.
No Study Drug
Researchers observe your health over time — no experimental treatment is given.
At a Glance
- Age
- 18 and older
- Sex
- Female
- Study type
- Observational
- Participants needed
- 12 (estimated)
- Sponsor
- University Hospital, Basel, Switzerland · Other
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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 identi…
Trial Locations
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Eligibility Criteria
Inclusion Criteria:
* Signed informed consent
* Age \> 18 years
* Proficient in German or Swiss German
* Category 2-4 Cesarean delivery under neuraxial anesthesia within last 48-72 hours
* Delivery of an healthy infant of at least 35+1 weeks of gestation
Exclusion Criteria:
* Known fetal abnormal…
Contacts