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Effect of B.Bifidum 900791 Intake in Adult With Hypolactasia and Lactose Intolerance

Effect of the Consumption of a Probiotic (B. Bifidum 900791)-Containing Ice-cream in Adult With Hypolactasia and Lactose Intolerance

Status
UNKNOWN
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT03952988
Enrollment
50
Registered
2019-05-16
Start date
2019-08-01
Completion date
2020-01-31
Last updated
2019-05-17

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Lactose Intolerance

Brief summary

Lactase is high in the newborn intestine, allowing him to digest the high amounts of lactose present in breastmilk. From weaning, lactase is genetically programmed to decrease, reaching residual levels in the adult. This situation occurs in 75% of the world population and is known as adult primary hypolactasia while the remaining 25% is lactase persistent i.e. maintains in adulthood lactase values similar to these of newborns. In subjects with hypolactasia, the intake of milk products can produce digestive symptoms, making that the affected individuals spontaneously reduce the consumption of these products and, therefore, their intake of calcium and proteins. In addition to lactose-free milk and exogenous lactase, a strategy for the intolerant subjects to continue consuming dairy products is, for example, to consume yogurt, due to the fact that the lactase of the yogurt bacteria continues to function in the intestine of the consumer, hydrolyzing lactose and decreasing the development of digestive symptoms. Similarly, many probiotic strains, such as L. acidophilus NCFM, L. casei CRL431, B. longum 401 and B. bifidum Orla Jensen 1424, express β-galactosidases that hydrolyze lactose, preventing its fermentation and the production of gases. The acute administration of these strains improves lactose tolerance. In addition, a recent study reported that dietary supplementation of intolerant subjects for 4 weeks with L. casei Shirota and B. breve Yakult reduced digestive symptoms and breath hydrogen excretion not only at the end of the period of administration of the probiotics but also 3 months after having discontinued the use of probiotics. Based on this background, the aim of this study is to determine whether the regular consumption of an ice cream with the strain B. bifidum 900791 improves lactose intolerance in hypolactasic subjects, even after the suspension of the consumption of the product. To determine if this effect is due to the adaptation of the microbiota, the investigators will also evaluate changes in the composition of the microbiota and the generation of volatile fatty acids.

Interventions

DIETARY_SUPPLEMENTProbiotic ice cream

One portion (50g) of an ice-cream containing the probiotic B. bifidum 900791 (\>10(exp7)/g) every day for 4 weeks

DIETARY_SUPPLEMENTPlacebo ice cream

One portion (50g) of an ice-cream without probiotic every day for 4 weeks

Sponsors

University of Chile
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
BASIC_SCIENCE
Masking
TRIPLE (Subject, Caregiver, Investigator)

Intervention model description

At Day 1, hypolactasic subjects will perform a Hydrogen Breath Test (HBT) with a placebo ice-cream with 20g lactose (Negative Control). A second HBT will be carried at Day-8 with the same product + an exogenous lactase (Positive control). A 3° HBT will be carried out at Day 15 with the probiotic ice cream with 20g lactose to determine the acute effect of the probiotic. Posteriorly, the subjects will be randomly assigned in one of 2 groups to consume an ice-cream/d, with or without the probiotic, for 4 weeks. At Day-43, they will carry out a 4° HBT with ice cream with 20g lactose and without probiotic (Evaluation of the chronic effect). At Day 71, after 4 weeks washout period, a 5° HBT will be carried out with the ice cream with lactose and without probiotic, to evaluate the remanence of the effect. A fresh stool will be obtained at days 15, 43 and 71 to determine the presence of the probiotic, microbiota composition, ß-galactosidase activity and short chain fatty acid concentrations.

Eligibility

Sex/Gender
ALL
Age
20 Years to 50 Years
Healthy volunteers
Yes

Inclusion criteria

* Diagnosis of hypolactasia and lactose intolerance

Exclusion criteria

* Diarrhea * Previous gastrointestinal pathologies * Current or recent intake of antibiotics, anti-inflammatory drugs, laxatives or drugs interfering with intestinal transit * Alterations of intestinal anatomy or function * Pregnancy * Chronic diseases of different etiologies (auto-immune, inflammatory, tumor, etc.).

Design outcomes

Primary

MeasureTime frameDescription
Area under curve (AUC) of hydrogen in the HBTDay 15Acute effect of the probiotic on hydrogen excretion after lactose ingestion

Secondary

MeasureTime frameDescription
Fecal microbiota alpha-diversityDays 15Shannon Index
Relative abundancies of the bacterial taxa forming the the fecal microbiotaDay 15Relative abundancies of the different bacterial taxa detected by high throughput sequencing
Fecal counts of B. bifidum 900791Days 15B. bifidum 900791 counts in fecal samples
Area under curve (AUC) of hydrogen in the HBTDay 43Chronic effect of the probiotic on hydrogen excretion after lactose ingestion
Fecal short chain fatty acids concentrationsDays 15Determination of short chain fatty acids concentrations in fecal samples
Scores of gastrointestinal symptoms: bloating, abdominal distention, abdominal pain, borborygms and flatulence, during the HBTDays 15Determination of gastrointestinal symptoms (bloating, abdominal distention, abdominal pain, borborygms and flatulence) using a previously validated questionnaire on a scale of 0 (none), 1 (mild), 2 (moderate), 3 (severe). We will define clinically relevant ymptoms as a composite score of 3 or more during the HBT.
Fecal beta-galactosidase activityDays 15Determination of the microbial beta-galactosidase activity in fecal samples (expressed as U/g)

Contacts

Primary ContactMartin Gotteland, PhD
mgottela@med.uchile.cl56-2-29786977
Backup ContactPamela Rojas, MD
projas@med.uchile.cl56-2-29786770

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026