4.2 Review

Ciprofol: A Novel Alternative to Propofol in Clinical Intravenous Anesthesia?

Journal

BIOMED RESEARCH INTERNATIONAL
Volume 2023, Issue -, Pages -

Publisher

HINDAWI LTD
DOI: 10.1155/2023/7443226

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Ciprofol, a novel compound developed in China, has been approved for sedation and anesthesia purposes. It has shown high efficacy, good selectivity, and minimal adverse reactions in clinical studies, indicating promising clinical application potential.
Ciprofol is a novel compound that was independently developed in China. According to the Chinese product instructions approved by the China National Medical Products Administration and the information of official website, indications for ciprofol include sedation and anesthesia during the surgical/procedure of nontracheal intubation, induction and maintenance of general anesthesia, and sedation during intensive care. Ciprofol is a short-acting intravenous sedative based on the structural modification of propofol. Ciprofol has high efficacy, good selectivity, and fewer adverse reactions, indicating good clinical application potential. A series of clinical studies have been conducted to evaluate the sedative effect of ciprofol in various procedures and settings, including gastroscopy and colonoscopy, fiber-optic bronchoscopy, general anesthesia in elective surgeries, and mechanical ventilation in intensive care units. This review summarizes the chemical structure, pharmacodynamics, and pharmacokinetic properties of ciprofol. We also assessed the efficacy and safety of ciprofol by synthesizing the relevant clinical trial data.

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