Ciprofol for heart protection during lung surgery
Part of Cancer, Lungs & breathing clinical trials.
This trial tests if a new sedative drug, Ciprofol, can reduce heart damage after non-cardiac surgery compared to standard care. It is for people aged 45–80 having planned lung surgery (like lobe removal or wedge resection) who will stay in the hospital for at least 3 days after the procedure.
Summary written for real people, not researchers, by Clin2.
Who can take part
- You are between 45 and 80 years old.
- You are scheduled for a planned lung surgery (such as removing part of your lung or a tumor) under general anesthesia.
- You are expected to stay in the hospital for at least 3 days after surgery.
- You are not allergic to propofol, Ciprofol, soy, eggs, or milk.
- You do not have unstable chest pain, heart failure, or severe lung or kidney disease.
- You are not pregnant, breastfeeding, or planning to conceive in the next 3 months.
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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