Institute for Translational Medicine, University of Pécs
Pécs, 7624, Hungary
NCT Number: NCT05100719
Irritable bowel syndrome (IBS) is a functional gastrointestinal disease. There is no well-defined pharmacological treatment. This clinical trial is a prospective, double-blind, two-armed randomized controlled, single-center trial. It is created to examine the role of IBS in patients with lactose intolerance. IBS patients undergo lactose H2 breath test (LHBT) and lactose tolerance test (LTT). Those with positive LTT and LHBT will be randomized into two groups: alverine-citrate + simethicone and lactase group (1) or alverin-citrate + simethicone with the placebo group (2). The goal of this study is to compare the lactase enzyme with placebo in IBS patients with lactose intolerance.
Trial opening soon.
Get Notified18 year–80 year
All sexes
Interventional
Not applicable
Pécs, 7624, Hungary
Irritable bowel syndrome (IBS) is one of the most frequently diagnosed gastroenterological disorders and can lead to significant deterioration of quality of life and an increase in health care and societal costs. Patients with lactose intolerance are unable to fully digest lactose caused by lactose malabsorption. The undigested lactose moves into the large intestine, fermented by bacteria, and causes bloating, gas, and diarrhea symptoms. The two, most frequently used diagnostic methods are the lactose H2 breath test (LHBT) and the lactose tolerance test (LTT). The restriction of lactose input or the replacement of the lactase enzyme can lead to the relief of the symptoms. Lactose intolerance is a common disorder among patients with IBS, it is more frequent than in the general population.
There are no studies that assess the link between lactose intolerance and IBS. Our primary objective is the examination of the relationship between lactose intolerance and IBS with or without the replacement of lactase enzyme. Our secondary objectives are to compare the lactase/beta-galactosidase enzyme replacement with placebo with the evaluation of a TSS (Total symptom score), VAS (Visual Analog Scale), QoL (Quality of life) questionnaires. The other secondary outcomes are to compare the severity of baseline symptoms during and after lactose administration.
Patients diagnosed with IBS according to the Rome IV criteria will test with LTT and LHBT.
Who has positive LTT and LHBT will randomize into two groups: (1) alverine-citrate + simethicone and lactase; (2) alverin-citrate + simethicone with placebo.
Healthy volunteers accepted: No
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
Exclusion criteria
Patients who randomized in the first arm are treated with alverine-citrate + simethicone and lactase.
Other names: lactase
Patients in the second arm receive alverin-citrate + simethicone with placebo without lactase.
Other names: placebo
Time frame: The one- and two-week total symptom score (TSS) change compared to baseline value.
The primary outcome is the number of enrolled patients with significant improvement in each treatment arm. Significant improvement is considered if there is >50% reduction in the TSS, compared to the baseline symptoms.
Time frame: The two time points at which the measurement is assessed are the time of enrollment and after 2 weeks.
stool consistency score of <5, according to the Bristol stool chart
Time frame: The three time points at which the measurement is assessed are the time of enrollment, after 1 and 2 weeks.
The absence of a bowel movement is accompanied by an improvement of ≥30 mm in the VAS (visual analogue scale) for the worst abdominal pain.
Time frame: The three time points at which the measurement is assessed are the time of enrollment, after 1 and 2 weeks.
The number of patients with acceptable relief of IBS-related bloating determined by a questionnaire, from the response (yes or no) compare to the baseline IBS-related bloating.
Time frame: The three time points at which the measurement is assessed are the time of enrollment, after 1 and 2 weeks.
Onset and duration of relief of bloating is measured by a questionnaire.
Time frame: At the time of patient enrollment and after two weeks of treatments this test will be carried out again.
Early (within 90 minutes), significant (≥20 ppm) H2 rise during LHBT or lactulose breath test compared to the baseline value.
Time frame: At the time of patient enrollment and after two weeks of treatments LHBT and LTT will be carried out again.
Results of LHBT (lactose H2 breath test) and LTT (lactose tolerance test).
University of Pecs
Other
The Role of Irritable Bowel Syndrome in Lactose Intolerance (LION Trial): Protocol of a Multicentre Randomized Controlled Clinical Trial
Acronym: LION
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