Monitoring pain and anxiety during planned cesarean delivery
Part of Mental health clinical trials.
This study is looking at how well a new, non-invasive monitor measures pain and anxiety in women during a planned cesarean delivery under spinal anesthesia. It may help doctors better understand and manage pain and anxiety during the procedure.
Summary written for real people, not researchers, by Clin2.
Who can take part
- You are a woman aged 18 or older.
- You are scheduled for an elective cesarean delivery with spinal anesthesia (numbing from the waist down).
- Your body mass index (BMI) is less than 35.
- You do not have a major psychiatric illness such as schizophrenia or bipolar disorder.
- You are not taking long-term medications for anxiety or other mental health conditions.
- You have no history of substance abuse and can communicate with the study team.
Quick eligibility check
Answer a few plain-language questions, based on this study's own requirements, to get a preliminary sense of fit.
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