Evidence map›Paper›PMID 31662866›Full record

Trial reportUnited European gastroenterology journal2019

Efficacy and safety of Gelsectan for diarrhoea-predominant irritable bowel syndrome: A randomised, crossover clinical trial.

Anca Trifan, Ovidiu Burta, Nicoleta Tiuca, Diana Corina Petrisor, Augustin Lenghel, Javier Santos

Open access · bronzeAbstract readComparative StudyMulticenter StudyRandomized Controlled Trial
In one paragraph

Trial report in United European gastroenterology journal, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 30 papers, 4 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
30citing papers in PubMed, 4 pooled it
4.6field-weighted citation impact, top 5% 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

30 citing papers in PubMed, 4 syntheses or guidelines pooled it, 52 citations in OpenAlex.

  1. Guideline
  2. Pooled it
  3. Pooled it
  4. Potential Benefit With Complementary and Alternative Medicine in Irritable Bowel Syndrome: A Systematic Review and Meta-analysis.Clinical gastroenterology and hepatology : the official clinical practice journal of the American Gastroenterological Association · 2021
    Pooled it
  5. Trial
  6. Trial
  7. Review
  8. A Topical Combination of Xyloglucan and Pea Protein Effectively Manages Oral Ulcers In Vivo.Journal of oral pathology & medicine : official publication of the International Association of Oral Pathologists and the American Academy of Oral Pathology · 2025
    Article
  9. Review
  10. Review
  11. Translational evaluation of GelsectanUnited European gastroenterology journal · 2024
    Article
  12. Review
  13. Future Therapies of Hepatic Encephalopathy.Clinics in liver disease · 2024
    Review
  14. Review
  15. Article
  16. Article
  17. Article
  18. Review
  19. Review
  20. 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 at 5 institutions in 3 countries.

Anca TrifanSC Gastromedica SRL, Iasi, Romania.
Ovidiu BurtaDepartment of Internal Medicine, Municipal Hospital Dr. Gavril Curteanu, Oradea, Romania.
Nicoleta TiucaDepartment of Internal Medicine, University Emergency Hospital Bucharest, Romania.
Diana Corina PetrisorEndodigest Medical Clinic, Oradea, Romania.
Augustin LenghelCMI Augustin Lenghel, Oradea, Romania.
Javier SantosDigestive System Research Unit, University Hospital Vall d'Hebron, Spain.
University of Oradea · ROAgora University · ROClinical Emergency Hospital Bucharest · ROHebron University · PSInstitutul Regional de Oncologie · RO

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background: Irritable bowel syndrome (IBS) is highly prevalent and presents a clinical challenge. Gelsectan is a medical device containing xyloglucan (XG), pea protein and tannins (PPT) from grape seed extract, and xylo-oligosaccharides (XOS), which act together to protect and reinforce the intestinal barrier. Objective: The objective of this study is to evaluate the efficacy and safety of XG + PPT + XOS in patients with diarrhoea-predominant IBS (IBS-D). Methods: In this double-blind study, 60 patients were randomly assigned to receive XG + PPT + XOS or placebo for 28 days, then crossed over to the alternative treatment. Patients were followed for 60 days. Results: At Day 28, a significantly higher proportion of patients starting treatment with XG + PPT + XOS than placebo (87 vs 0%; Conclusion: XG + PPT + XOS effectively controlled diarrhoea and alleviated clinical symptoms in patients with IBS-D, and was well tolerated.

Indexed as

Abdominal PainAdultCross-Over StudiesDemulcentsDiarrheaDouble-Blind MethodDrug Therapy, CombinationEquipment DesignFemaleFollow-Up StudiesGlucansHumansIrritable Bowel SyndromeMaleOligosaccharidesPea ProteinsDemulcentsGlucansOligosaccharidesPea ProteinsPlacebosPrebioticsXylansxyloglucanDiarrhoea-predominant irritable bowel syndromeGelsectanmucoprotectantspea protein and tanninsprebioticsxyloglucanxylo-oligosaccharide

Identifiers

PMID31662866
PMCPMC6794699
OpenAlexW2956126375

What OpenQuestion holds

Textmetadata
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.