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

United European Gastroenterol J. 2019 Oct;7(8):1093-1101. doi: 10.1177/2050640619862721. Epub 2019 Jul 3.

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%; p = 0.0019) presented normal stools (Bristol Stool Form Scale type 3-4). At Day 56, a significantly higher proportion of patients who crossed over to XG + PPT + XOS than placebo (93% vs 23%; p = 0.0001) presented normal stools. In the group allocated to receive XG + PPT + XOS after placebo, benefits of XG + PPT + XOS were maintained during follow-up. Subjective assessments of abdominal pain, bloating, quality of life and general health indicated significant improvement with XG + PPT + XOS over placebo. There were no related adverse events.

Conclusion: XG + PPT + XOS effectively controlled diarrhoea and alleviated clinical symptoms in patients with IBS-D, and was well tolerated.

Keywords: Diarrhoea-predominant irritable bowel syndrome; Gelsectan; mucoprotectants; pea protein and tannins; prebiotics; xylo-oligosaccharide; xyloglucan.

Publication types

  • Comparative Study
  • Multicenter Study
  • Randomized Controlled Trial
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Abdominal Pain / diagnosis
  • Abdominal Pain / drug therapy
  • Abdominal Pain / etiology
  • Adult
  • Cross-Over Studies
  • Demulcents / administration & dosage
  • Demulcents / therapeutic use*
  • Diarrhea / drug therapy*
  • Double-Blind Method
  • Drug Therapy, Combination
  • Equipment Design / instrumentation
  • Female
  • Follow-Up Studies
  • Glucans / administration & dosage
  • Glucans / therapeutic use*
  • Humans
  • Irritable Bowel Syndrome / complications
  • Irritable Bowel Syndrome / diagnosis*
  • Irritable Bowel Syndrome / epidemiology
  • Irritable Bowel Syndrome / psychology
  • Male
  • Oligosaccharides / administration & dosage
  • Oligosaccharides / therapeutic use*
  • Pea Proteins / administration & dosage
  • Pea Proteins / therapeutic use*
  • Placebos / administration & dosage
  • Prebiotics / administration & dosage
  • Prevalence
  • Quality of Life
  • Romania / epidemiology
  • Safety
  • Treatment Outcome
  • Xylans / administration & dosage
  • Xylans / therapeutic use*

Substances

  • Demulcents
  • Glucans
  • Oligosaccharides
  • Pea Proteins
  • Placebos
  • Prebiotics
  • Xylans
  • xyloglucan

Associated data

  • EudraCT/2016-004832-40