Trial reportPeerJ2026
Impact of reducing the duration of fasting and no drinking on the experiences of older patients receiving painless gastroscopy: a randomized controlled trial.
Trial report in PeerJ, 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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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
12 authors.
Funding
No grant is acknowledged in the PubMed record.
Abstract
Background: Before undergoing painless gastroscopy, patients are required to fast and no drinking for at least 4 h which is unpleasant for older patients. Objective: The aim of this study is to increase the preprocedural comfort of older patients by reducing the duration of fasting and no drinking before painless gastroscopy while ensuring safety. Methods: Older patients aged more than 65 years who underwent painless gastroscopy were randomly allocated to the study group ( Results: In the study group, the incidence of thirst, hunger, dizziness, and fatigue before gastroscopy was significantly lower than that in the control group (33.4% Conclusion: In this random trial of older patients undergoing painless gastroscopy, ingestion of 250 ml opaque liquid 4 h before, followed by 250 ml water 2 h before, improved pre-procedure comfort and patient satisfaction compared with conventional fasting. We observed no statistically significant increase in clinically identified gastric reflux, aspiration, or impaired endoscopic field clarity; however, the incidence of such adverse events was low, and the trial was not powered to exclude small increases in rare but serious complications. Larger studies would be required to definitively establish safety equivalence.
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