Trial reportBMC anesthesiology2025
Comparison of intravenous nalbuphine and sufentanil on the median effective effect-site concentration of propofol to attenuate the response to cervical dilation during hysteroscopy: a double-blind, dose-response study.
Trial report in BMC anesthesiology, 2025. 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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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.
The trial behind it
Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.
Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.
Who cites it
0 citing papers in PubMed.
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Corrections and comments
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Authors and funding
8 authors.
Funding
No grant is acknowledged in the PubMed record.
Abstract
backgroundNalbuphine, a synthetic opioid receptor agonist, exhibits comparable analgesic activity to morphine while demonstrating superior safety. Recent reports suggest that it is more effective than sufentanil in relieving uterine contraction pain. The objective of our study was to investigate the role of nalbuphine in reducing effect-site propofol concentration (Ce
methodsNinety patients having monitored anesthesia care for hysteroscopy were randomized to receive 0.15 mg·kg
resultsThe calculated EC
conclusionsDuring hysteroscopic surgery, when compared with sufentanil, 0.2 mg·kg
trial registrationThe study was then registered on August 9th, 2023 at the Chinese Clinical Trial Registry which participates in the World Health Organization International Clinical Trials Registry Platform (Identifier: ChiCTR2300074513) before enrolling the first participant and written informed consent was obtained by each patient.
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