David Gunn
Randomised, placebo-controlled trial and meta-analysis show benefit of ondansetron for irritable bowel syndrome with diarrhoea: The TRITON trial
Gunn, David; Topan, Rabia; Barnard, Lorna; Fried, Ron; Holloway, Ivana; Brindle, Richard; Corsetti, Maura; Scott, Mark; Farmer, Adam; Kapur, Kapil; Sanders, David; Eugenicos, Maria; Trudgill, Nigel; Whorwell, Peter; Mclaughlin, John; Akbar, Ayesha; Houghton, Lesley; Dinning, Phil G.; Aziz, Qasim; Ford, Alexander C.; Farrin, Amanda J.; Spiller, Robin
Authors
Rabia Topan
Lorna Barnard
Ron Fried
Ivana Holloway
Richard Brindle
Dr MAURA CORSETTI Maura.Corsetti@nottingham.ac.uk
CLINICAL ASSOCIATE PROFESSOR
Mark Scott
Adam Farmer
Kapil Kapur
David Sanders
Maria Eugenicos
Nigel Trudgill
Peter Whorwell
John Mclaughlin
Ayesha Akbar
Lesley Houghton
Phil G. Dinning
Qasim Aziz
Alexander C. Ford
Amanda J. Farrin
Professor ROBIN SPILLER ROBIN.SPILLER@NOTTINGHAM.AC.UK
PROFESSOR OF GASTROENTEROLOGY
Abstract
Summary: Background: Ondansetron may be beneficial in irritable bowel syndrome with diarrhoea (IBS‐D). Aim: To conduct a 12‐week parallel group, randomised, double‐blind, placebo‐controlled trial of ondansetron 4 mg o.d. (titrated up to 8 mg t.d.s.) in 400 IBS‐D patients. Primary endpoint: % responders using the Food and Drug Administration (FDA) composite endpoint. Secondary and mechanistic endpoints included stool consistency (Bristol Stool Form Scale) and whole gut transit time (WGTT). After literature review, results were pooled with other placebo‐controlled trials in a meta‐analysis to estimate relative risks (RR), 95% confidence intervals (CIs) and number needed to treat (NNT). Results: Eighty patients were randomised. On intention‐to‐treat analysis, 15/37 (40.5%; 95% CI 24.7%–56.4%) met the primary endpoint on ondansetron versus 12/43 (27.9%; 95% CI 14.5%–41.3%) on placebo (p = 0.19). Ondansetron improved stool consistency compared with placebo (adjusted mean difference − 0.7; 95% CI −1.0 to−0.3, p < 0.001). Ondansetron increased WGTT between baseline and week 12 (mean (SD) difference 3.8 (9.1) hours, versus placebo −2.2 (10.3) hours, p = 0.01). Meta‐analysis of 327 patients from this, and two similar trials, demonstrated ondansetron was superior to placebo for the FDA composite endpoint (RR of symptoms not responding = 0.86; 95% CI 0.75–0.98, NNT = 9) and stool response (RR = 0.65; 95% CI 0.52–0.82, NNT = 5), but not abdominal pain response (RR = 0.95; 95% CI 0.74–1.20). Conclusions: Although small numbers meant the primary endpoint was not met in this trial, when pooled with other similar trials meta‐analysis suggests ondansetron improves stool consistency and reduces days with loose stool and urgency. Trial registration – http://www.isrctn.com/ISRCTN17508514
Citation
Gunn, D., Topan, R., Barnard, L., Fried, R., Holloway, I., Brindle, R., Corsetti, M., Scott, M., Farmer, A., Kapur, K., Sanders, D., Eugenicos, M., Trudgill, N., Whorwell, P., Mclaughlin, J., Akbar, A., Houghton, L., Dinning, P. G., Aziz, Q., Ford, A. C., …Spiller, R. (2023). Randomised, placebo-controlled trial and meta-analysis show benefit of ondansetron for irritable bowel syndrome with diarrhoea: The TRITON trial. Alimentary Pharmacology and Therapeutics, 57(11), 1258-1271. https://doi.org/10.1111/apt.17426
Journal Article Type | Article |
---|---|
Acceptance Date | Feb 7, 2023 |
Online Publication Date | Mar 3, 2023 |
Publication Date | 2023-06 |
Deposit Date | Feb 9, 2023 |
Publicly Available Date | Mar 4, 2024 |
Journal | Alimentary Pharmacology and Therapeutics |
Print ISSN | 0269-2813 |
Electronic ISSN | 1365-2036 |
Publisher | Wiley |
Peer Reviewed | Peer Reviewed |
Volume | 57 |
Issue | 11 |
Pages | 1258-1271 |
DOI | https://doi.org/10.1111/apt.17426 |
Keywords | Pharmacology (medical); Gastroenterology; Hepatology |
Public URL | https://nottingham-repository.worktribe.com/output/17082601 |
Publisher URL | https://onlinelibrary.wiley.com/doi/10.1111/apt.17426 |
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Randomised, placebo-controlled trial and meta-analysis show benefit of ondansetron for irritable bowel syndrome with diarrhoea: The TRITON trial
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Copyright Statement
© 2023 The Authors. Alimentary Pharmacology & Therapeutics published by John Wiley & Sons Ltd.
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