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The Effect of Probioticson Bloating in IBS

R

Royal Veterinary and Agricultural University, Denmark

Status

Unknown

Conditions

Irritable Bowel Syndrome

Treatments

Drug: Probiotic bacteria (Trevis R)

Study type

Interventional

Funder types

Other

Identifiers

Details and patient eligibility

About

The purpose of the study is to establish an in-vitro method to evaluate the effect of probiotics on gas production in feces (hydrogen and methane)

Full description

The objective of this study is to establish a model for screening probiotic bacteria in the treatment of meteorism symptoms (feeling of air in the stomach) with otherwise healthy adult women. As excessive bacterial gas production in the intestine is the most likely mechanism behind meteorism, we will examine eventual changes of the production of gases (hydrogen and methane) before and after administration of Trevis®. For screening of Trevis® we will apply a combination of clinical examination and a laboratory model for the determination of gastrointestinal gas production (a new method in connection with studies on probiotics). The results will be compared with the test person's specification of their health, both with respect to gastrointestinal function and in general through questionnaires. The background for the project will be described in the following.

Sex

Female

Ages

18+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Female test persons with symptoms of meteorism, the age of > 18 years, completely integrated in the Danish society (including nutrition), and no previous abdominal surgery besides from appendicectomy (advertisement in a local newspaper for test persons).

Exclusion criteria

  • Lactose and sorbitol intolerant persons (based on hydrogen breath tests).
  • Persons with chronic ingestion of medicine, that might have an effect on gut bacterial flora or bowel motility.
  • Persons taking antibiotics within 2 month prior to the trial
  • Persons with diagnosed gastrointestinal disease other than IBS.
  • Persons not able to understand and/or read Danish.
  • Persons under age and persons with obvious problems remembering and sticking to the protocol (persons with dementia, psychological illness etc.)

Trial design

Primary purpose

Treatment

Allocation

Randomized

Interventional model

Crossover Assignment

Masking

Double Blind

Trial contacts and locations

1

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Central trial contact

Julie Schrøder, student; Jens R Andersen, MD

Data sourced from clinicaltrials.gov

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