Evidence map›Paper›PMID 41987769›Full record

Trial reportFrontiers in medicine2026

Age-related reduction in ciprofol requirement for loss of consciousness during anesthesia induction: a prospective cohort study.

Yu-Gang Lu, Fa-Qiang Zhang, Yi-Yu He, Tong Ding, Fang Deng, Wen Liu, Jin-Chao Song

Abstract readClinical Trial
In one paragraph

Trial report in Frontiers in medicine, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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1 · What the graph read from it

What it found

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The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

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3 · Its place in the literature

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0 citing papers in PubMed.

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4 · The record

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5 · Who and what money

Authors and funding

7 authors.

Yu-Gang Lu *Department of Anesthesiology, Shanghai Pulmonary Hospital, Tongji University School of Medicine, Shanghai, China.
Fa-Qiang Zhang *Department of Anesthesiology and Perioperative Medicine, Shanghai Fourth People's Hospital, Tongji University School of Medicine, Shanghai, China.
Yi-Yu He *Department of Anesthesiology, Shidong Hospital Affiliated to University of Shanghai for Science and Technology, Shanghai, China.
Tong DingDepartment of Anesthesiology, Shidong Hospital Affiliated to University of Shanghai for Science and Technology, Shanghai, China.
Fang DengDepartment of Anesthesiology, Shidong Hospital Affiliated to University of Shanghai for Science and Technology, Shanghai, China.
Wen LiuDepartment of Anesthesiology, Shidong Hospital Affiliated to University of Shanghai for Science and Technology, Shanghai, China.
Jin-Chao SongDepartment of Anesthesiology, Shidong Hospital Affiliated to University of Shanghai for Science and Technology, Shanghai, China.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background: Ciprofol, a novel intravenous anesthetic for procedural sedation and general anesthesia, characterized by rapid onset of action, lower rates of injection pain and effective sedation at lower doses, is a promising alternative to propofol. Further clinical evidence is needed on how to adjust the dosage regimen of ciprofol during anesthesia induction in elderly patients. This study aims to provide evidence-based dosing reference and investigate the correlation between patient age and the ciprofol requirement for loss of consciousness (LOC) during anesthesia induction. Methods: A total of 102 patients scheduled for elective surgery under general anesthesia were enrolled and grouped to Group A (51 patients, 18-64 years) and Group B (51 patients, ≥65 years) according to their age. All subjects received ciprofol (at a rate of 5 mg/kg/min) alone for inducing LOC, which was defined as loss of eyelash reflex and Modified Observer's Alertness/Sedation (MOAA/S) score of 1 or less. The dose of ciprofol and the time to loss of eyelash reflex for each subject were recorded. Results: Compared with patients in group A, patients in group B had a mean reduction in ciprofol requirement of 0.07 mg/kg and a mean reduction in the time to loss of eyelash reflex of 55.20 s. Bivariate linear correlation analysis showed that ciprofol requirement for LOC was significantly and positively correlated with albumin ( Conclusion: The ciprofol requirement for LOC was significantly reduced in elderly patients. Our findings demonstrated that age serves as an independent factor influencing the ciprofol requirement for LOC during general anesthesia induction. These results suggest that the induction dose of ciprofol should be further reduced in elderly surgical patients, particularly those aged 75 years or older. Clinical trial registration: https://www.chictr.org.cn/; Identifier: ChiCTR2400093112.

Indexed as

anestheticsciprofolelderlyintravenous anesthesialoss of consciousness

Identifiers

PMID41987769
PMCPMC13076542

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.