Evidence map›Paper›PMID 36362815›Full record

ArticleJournal of clinical medicine2022

Effects of Microencapsulated Sodium Butyrate, Probiotics and Short Chain Fructooligosaccharides in Patients with Irritable Bowel Syndrome: A Study Protocol of a Randomized Double-Blind Placebo-Controlled Trial.

Anita Gąsiorowska, Marek Romanowski, Ewa Walecka-Kapica, Aleksandra Kaczka, Cezary Chojnacki, Milena Padysz, Marta Siedlecka, Joanna B Bierła, Robert E Steinert, Bożena Cukrowska

Open access · goldAbstract read
In one paragraph

Article in Journal of clinical medicine, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers.

0numbers the graph read from it
0cells of the map it votes in
10citing papers in PubMed
2.0field-weighted citation impact, top 14% of its field
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.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

10 citing papers in PubMed, 12 citations in OpenAlex.

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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

10 authors at 3 institutions in 2 countries.

Anita GąsiorowskaGastroenterology Department, Medical University of Lodz, ul. Pomorska 251, 92-213 Łódź, Poland.
Marek RomanowskiGastroenterology Department, Medical University of Lodz, ul. Pomorska 251, 92-213 Łódź, Poland.
Ewa Walecka-KapicaGastroenterology Department, Medical University of Lodz, ul. Pomorska 251, 92-213 Łódź, Poland.
Aleksandra KaczkaGastroenterology Department, Medical University of Lodz, ul. Pomorska 251, 92-213 Łódź, Poland.
Cezary ChojnackiGastroenterology Department, Medical University of Lodz, ul. Pomorska 251, 92-213 Łódź, Poland.ORCID 0000-0002-1620-4775
Milena PadyszGastroenterology Department, Medical University of Lodz, ul. Pomorska 251, 92-213 Łódź, Poland.ORCID 0000-0002-8973-577X
Marta SiedleckaGastroenterology Department, Medical University of Lodz, ul. Pomorska 251, 92-213 Łódź, Poland.
Joanna B BierłaDepartment of Pathomorphology, The Children's Memorial Health Institute, Aleja Dzieci Polskich 20, 04-730 Warsaw, Poland.ORCID 0000-0002-5772-5091
Robert E SteinertDSM Nutritional Products Ltd., P.O. Box 2676, 4002 Basel, Switzerland.ORCID 0000-0001-7884-5036
Bożena CukrowskaDepartment of Pathomorphology, The Children's Memorial Health Institute, Aleja Dzieci Polskich 20, 04-730 Warsaw, Poland.ORCID 0000-0001-6887-0094
Medical University of Lodz · PLChildren's Memorial Health Institute · PLUniversity Hospital of Zurich · CH

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Irritable bowel syndrome (IBS) is a functional gastrointestinal disease in the pathogenesis of which gut dysbiosis may play an important role. Thus, probiotics, prebiotics, or microbiota metabolites, such as butyric acid, are considered to be effective therapy for IBS. However, there are still no trials presenting the efficacy of these three biotic components administered simultaneously. This study aims to evaluate the effects of the product comprising sodium butyrate, probiotics, and short-chain fructooligosaccharides (scFOS) on the severity of clinical IBS symptoms and the quality of life (IBS-QOL). This is a randomized double-blind placebo-controlled trial conducted in 120 adults with IBS diagnosed according to Rome IV criteria. The intervention group (n = 60) will receive a mixture of the following components: 300 mg of colon-targeted microencapsulated sodium butyrate combined with probiotic

Indexed as

butyric acidirritable bowel syndromeprebioticsprobioticsstudy protocol

Identifiers

PMID36362815
PMCPMC9655302
OpenAlexW4308510068

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

None linked

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.