Evidence map›Paper›PMID 24147869›Full record

Trial reportInternational journal of clinical practice2014

On-demand treatment with alverine citrate/simeticone compared with standard treatments for irritable bowel syndrome: results of a randomised pragmatic study.

P Ducrotte, J C Grimaud, M Dapoigny, S Personnic, V O'Mahony, M C Andro-Delestrain

2 registry-linked trialsAbstract readComparative StudyMulticenter StudyPragmatic Clinical Trial
In one paragraph

Trial report in International journal of clinical practice, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to 2 registered trials, which are not on this map. Cited by 9 papers.

0numbers the graph read from it
0cells of the map it votes in
9citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

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

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.

NCT01404923 phase4completednot on this map

Assessment of On-demand MeteoSpasmyl® Use Effectiveness in Irritable Bowel Syndrome

TypeinterventionalSponsorLaboratoires Mayoly SpindlerRan2009 to 2011Enrolled436ConditionsIrritable Bowel SyndromeArmsanti spasmodic agents, alverine citrate, simeticone
NCT05100719 nanot yet recruitingnot on this mapstarted 2022, after this paper: background citation

The Role of Irritable Bowel Syndrome in Lactose Intolerance (LION Trial): Protocol of a Multicentre Randomized Controlled Clinical Trial

TypeinterventionalSponsorUniversity of PecsRan2022 to 2026Enrolled200ConditionsIrritable Bowel Syndrome, Lactose Intolerance, Lactose MalabsorptionArmsalverine-citrate + simethicone and lactase, alverin-citrate + simethicone with placebo
3 · Its place in the literature

Who cites it

9 citing papers in PubMed.

  1. Trial
  2. Trial
  3. Review
  4. Expert Opinion on the Efficacy and Safety of Antispasmodics with a Focus on Irritable Bowel Syndrome.The Turkish journal of gastroenterology : the official journal of Turkish Society of Gastroenterology · 2025
    Review
  5. Review
  6. Article
  7. Review
  8. Article
  9. Review
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

6 authors.

P DucrotteDepartment of Gastroenterology, UMR 1073, Rouen University Hospital, University of Rouen, Rouen, France.
J C Grimaud
M Dapoigny
S Personnic
V O'Mahony
M C Andro-Delestrain

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundIn routine practice, irritable bowel syndrome (IBS) symptoms are often difficult to be relieved and impair significantly patients' quality of life (QoL). A randomised, double-blind, placebo-controlled study has shown the efficacy of alverine citrate/simeticone (ACS) combination for IBS symptom relief.

aimAs IBS symptoms are often intermittent, this pragmatic study was designed to compare the efficacy of an on-demand ACS treatment vs. that of usual treatments.

methodsRome III IBS patients were enrolled by 87 general practitioners who were randomly allocated to one of two therapeutic strategies: on-demand ACS or usual treatment chosen by the physician. The primary outcome measure was the improvement of the IBSQoL score between inclusion and month 6.

resultsA total of 436 patients (mean age: 54.4 years; women: 73.4%) were included, 222 in the ACS arm and 214 patients in the usual treatment arm, which was mainly antispasmodics. At 6 months, improvement of IBSQoL was greater with ACS than with the usual treatment group (13.8 vs. 8.4; p < 0.0008). The IBS-severity symptom score (IBS-SSS) was lower with ACS than in the usual treatment arm with a mean (SE) decrease of 170.0 (6.6) vs. 110.7 (6.7), respectively (p = 0.0001). An IBS-SSS < 75 was more frequent in the ACS group (37.7% vs. 16.0%; p < 0.0001). Improvement of both abdominal pain and bloating severity was also greater with the on-demand ACS treatment, which was associated with both lower direct and indirect costs.

conclusionsAfter 6 months, on-demand ACS treatment led to a greater improvement of QoL, reduced the burden of the disease and was more effective for IBS symptom relief than usual treatments.

Indexed as

Abdominal PainAntifoaming AgentsDouble-Blind MethodDrug CombinationsFemaleHumansIrritable Bowel SyndromeMaleMiddle AgedPropylaminesQuality of LifeSerotonin Receptor AgonistsSimethiconeTreatment OutcomealverineAntifoaming AgentsDrug CombinationsPropylaminesSerotonin Receptor AgonistsSimethicone

Identifiers

PMID24147869
PMCPMC4282257

What OpenQuestion holds

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Registered trials

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.