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ArticleDigestive diseases and sciences2026

Low-Dose Naltrexone in Crohn's Disease: A Prematurely Terminated Randomized Trial Showing Reduced Fatigue Without Clinical or Endoscopic Benefit.

N van de Pol, E Paulides, F H J Wolfhagen, R L West, I L Holster, K E Verweij, A C de Vries, G M Fuhler, C J van der Woude

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Article in Digestive diseases and sciences, 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.

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3 · Its place in the literature

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4 · The record

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5 · Who and what money

Authors and funding

9 authors.

N van de PolDepartment of Gastroenterology and Hepatology, Erasmus University Medical Center, Dr. Molewaterplein 40, PO Box 2040, 3015GD, Rotterdam, the Netherlands. n.vandepol@erasmusmc.nl.ORCID https://orcid.org/0000-0002-4699-6662
E PaulidesDepartment of Gastroenterology and Hepatology, Erasmus University Medical Center, Dr. Molewaterplein 40, PO Box 2040, 3015GD, Rotterdam, the Netherlands.
F H J WolfhagenDepartment of Gastroenterology and Hepatology, Albert Schweitzer Hospital, Dordrecht, the Netherlands.
R L WestDepartment of Gastroenterology and Hepatology, Franciscus, Rotterdam, the Netherlands.
I L HolsterDepartment of Gastroenterology and Hepatology, Maasstad Hospital, Rotterdam, the Netherlands.
K E VerweijDepartment of Gastroenterology and Hepatology, Maasstad Hospital, Rotterdam, the Netherlands.
A C de VriesDepartment of Gastroenterology and Hepatology, Erasmus University Medical Center, Dr. Molewaterplein 40, PO Box 2040, 3015GD, Rotterdam, the Netherlands.
G M FuhlerDepartment of Gastroenterology and Hepatology, Erasmus University Medical Center, Dr. Molewaterplein 40, PO Box 2040, 3015GD, Rotterdam, the Netherlands.
C J van der WoudeDepartment of Gastroenterology and Hepatology, Erasmus University Medical Center, Dr. Molewaterplein 40, PO Box 2040, 3015GD, Rotterdam, the Netherlands.

Funding

ZonMw 848082001
6 · The paper itself

Abstract

backgroundCrohn's disease (CD) is often refractory to standard therapies, and patients are sometimes reluctant to initiate immunosuppressive therapy, prompting interest in novel treatments such as low-dose naltrexone (LDN).

aimsTo evaluate the efficacy of LDN for induction of remission in patients with mild-to-moderate active CD.

methodsWe conducted a multicenter, double-blind, placebo-controlled trial in 7 hospitals in the Netherlands. Adults with active CD (defined by mucosal ulcers on endoscopy and Simple endoscopic score for CD 3-15) were randomized 1:1 to LDN 4.5 mg once daily or placebo for 12 weeks. The primary endpoint was endoscopic remission at week 12. Secondary endpoints included clinical and endoscopic response, safety and patient-reported outcome measures. The trial was stopped early due to futility.

resultsForty-one patients were randomized. After 12 weeks, endoscopic remission occurred in 1 (5.6%) vs. 3 (18.8%) patients for LDN and placebo (p=0.233), respectively. Clinical remission occurred in 22.2% (LDN) vs. 70.0% (placebo) (p=0.037). No serious adverse events were reported. For the FACIT-Fatigue questionnaire, the median difference after 12 weeks was 2.5 (IQR 0-7) for LDN vs. -3 (IQR -7-2) for placebo (p=0.012). Additionally, patient-reported outcomes showed no significant difference between LDN and placebo.

conclusionsLDN was not effective for inducing remission in CD and showed no benefit over placebo. Despite not being an effective treatment for clinical and endoscopic outcomes, it may enhance better quality of life by reducing fatigue symptoms. Future studies are needed to clarify its potential benefit on fatigue in patients with inflammatory bowel disease.

Indexed as

Crohn’s diseaseFatigueInflammatory bowel diseaseLow-dose naltrexoneQuality of life

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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.