Effect of Probiotic Supplementation on Lactose Maldigestion Induced by Lactose Solution

Lactose Intolerance Clinical Trial

Official title:

Effect of Probiotic Supplementation on Lactose Maldigestion Induced by Lactose Solution: Randomized, Double-blind, Placebo-controlled, Positive-controlled, Three-way Crossover, Acute Lactose Challenge

Clinical Trial Details — Status: Completed

Administrative data

• NCT number: NCT03814668
• Other study ID #: NH-03978
• Status: Completed
• Phase: N/A
• Start date: November 5, 2018
• Est. completion date: April 30, 2019

Study information

• Verified date: August 2019
• Source: Danisco
• Contact: n/a
• Is FDA regulated: No
• Study type: Interventional

Clinical Trial Summary

Study objectives:

Primary:

Difference in breath hydrogen concentration (BHC, ppm) in lactase and probiotic groups compared to placebo, measured by the incremental area under curve (iAUC) analysis

Non-inferiority in breath hydrogen concentration (BHC, ppm) of probiotic group compared to lactase group, measured by the incremental area under curve (iAUC) analysis

Secondary:

Breath test

• Breath hydrogen peak value (ppm) in lactase and probiotic groups compared to placebo

• Cumulative breath hydrogen (ppm) in lactase and probiotic groups compared to placebo

Acute gastrointestinal symptoms (severity or presence/absence to be defined on a Likert scale) in lactase and probiotic groups compared to placebo

• Abdominal pain

• Flatulence

• Bloating

• Nausea and vomiting

• Bowel movements and diarrhea (if present, stool consistency to be defined on Bristol stool scale and number of bowel movements to be recorded)

Ancillary:

• Baseline fasting BHC (ppm)

• Breath methane CH4 (ppm)

• Breath carbon dioxide CO2 (ppm)

• Probiotic identification in feces before each lactose challenge by molecular methods

• Gene test to determine lactase deficiency status at screening (following SNP variants to be screened: 13910*C (Europe, Central Asia, commonly used) -22018*G (Europe), -13915*T (Saudi-Arabia, Africa), -14010*G (Africa), -13907*C (Africa))

Recruitment information / eligibility

• Status: Completed
• Enrollment: 34
• Est. completion date: April 30, 2019
• Est. primary completion date: April 30, 2019
• Accepts healthy volunteers: Accepts Healthy Volunteers
• Gender: All
• Age group: 25 Years to 65 Years

Eligibility

Inclusion Criteria:

1. Voluntary, written, informed consent to participate in the study

2. Agreement to comply with the protocol and study restrictions

3. Healthy females and males of age 25 to 60 years (inclusive)

4. Self-declared, suspected or medically diagnosed lactose intolerance

5. Increase of more than 20 ppm in breath hydrogen within 3 h from the baseline fasting breath hydrogen value

6. Participants who agree to maintain their usual dietary habits throughout the trial period

7. Participants who agree not to consume probiotics, prebiotics, fermented milk, and/or yogurt containing probiotics during the intervention period (Visits 3-5) and two weeks before Visit 3 (2 weeks after screening visit)

8. Females of child-bearing potential who agree to use a medically approved method of birth control

9. Ability of the participant (in the investigator's opinion) to comprehend the full nature and purpose of the study including possible risks and side effects

10. Covered by Health Insurance System and / or in compliance with the recommendations of National Law in force relating to biomedical research

Exclusion Criteria:

1. Gastrointestinal disorder or disease (e.g. Crohn's disease, ulcer, irritable bowel syndrome (IBS), Celiac disease, small intestinal bacterial overgrowth (SIBO), pancreatitis and disorders affecting gastrointestinal motility)

2. Diagnosed type 1 or type 2 diabetes

3. Prior abdominal surgery that, in the opinion of the investigator, may present a risk for the participant or affect study results

4. Ongoing or recent (last 1 month) antibiotic treatment.

5. Use of laxatives or drugs known to affect gut motility 1 month preceding the screening visit and during the study

6. Ongoing or recurrent use of proton pump inhibitors

7. Colonoscopy within 3 months before screening

8. History of recurrent colon cleansing and/or a colon cleansing within 3 months before screening

9. Gastrointestinal infection within 1 month before screening or during the trial

10. Clinically significant underlying systemic illness that may preclude the participant's ability to complete the trial or that may affect the study outcomes (e.g. bowel cancer, prostate cancer, terminal illness)

11. History of diagnosed coronary heart disease/cardiovascular disease or artificial heart valve

12. Any obstructive or restrictive respiratory syndrome/disease that may impact breath test (e.g. asthma or chronic obstructive pulmonary disease (COPD))

13. Regular use of tobacco, snuff, nicotine and e-cigarette, and possible other inhaled products. Light smokers (less than 5 cigarettes per day) who agree not to smoke during the whole duration of the study may be included.

14. Self-declared history of alcohol abuse (for females: >3 drinks on any single day and >7 drinks per week; for males: >4 drinks on any single day and >14 drinks per week)

15. Self-declared use of illicit drugs within 4 weeks preceding the screening visit

16. Pregnant or lactating female, or pregnancy planned during study period

17. Participants under administrative or legal supervision.

18. Participation in another study with any investigational product within 60 days of screening

19. Clinically significant abnormal values in safety blood tests at screening

20. Other reasons that, in the opinion of the Investigator, make the participant unsuitable for enrolment

21. Who would receive more than 4500€ as indemnities for his participation in biomedical research within the last 12 months, including the indemnities for the present study.

Related Conditions & MeSH terms

• Lactose Intolerance

Intervention

Dietary Supplement:
• Probiotic
Intake of probiotic
• Lactase
Intake of lactase

Other:
• Placebo
Intake of placebo

Locations

Country	Name	City	State
France	Eurofins Optimed	Gières

Sponsors (1)

Lead Sponsor	Collaborator
Danisco

Country where clinical trial is conducted

France, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Other	Difference in baseline fasting BHC (ppm) between the treatments	Difference in baseline fasting BHC (ppm) between the treatments	Baseline
Other	Difference in breath methane concentration (ppm) between the treatments	Difference in breath methane concentration (ppm) between the treatments	During the 6-hour acute lactose challenge
Other	Difference in breath carbon dioxide concentration (ppm) between the treatments	Difference in breath methane concentration (ppm) between the treatments	During the 6-hour acute lactose challenge
Other	Difference in the quantity of probiotic in fecal samples between the treatments	Difference in the quantity of probiotic in fecal samples between the treatments	48-hours before the visits
Other	Description of the SNP variants in each treatment group	Description of the SNP variants in each treatment group	At screening
Primary	Difference in breath hydrogen concentration (BHC, ppm) in probiotic group compared to placebo	Difference in breath hydrogen concentration (BHC, ppm) in probiotic compared to placebo, measured by the iAUC analysis	During the 6-hour acute lactose challenge
Primary	Difference in breath hydrogen concentration (BHC, ppm) in lactase group compared to placebo	Difference in breath hydrogen concentration (BHC, ppm) in lactase group compared to placebo, measured by the iAUC analysis	During the 6-hour acute lactose challenge
Primary	Non-inferiority in breath hydrogen concentration (BHC, ppm) of probiotic group compared to lactase group (positive control)	Non-inferiority in breath hydrogen concentration (BHC, ppm) of probiotic group compared to lactase group (positive control), measured by the iAUC analysis	During the 6-hour acute lactose challenge
Secondary	Difference in breath hydrogen concentration (BHC, ppm) in lactase group compared to placebo, measured by breath hydrogen peak value	Difference in breath hydrogen concentration (BHC, ppm) in lactase group compared to placebo, measured by breath hydrogen peak value	During the 6-hour acute lactose challenge
Secondary	Difference in breath hydrogen concentration (BHC, ppm) in probiotic group compared to placebo, measured by breath hydrogen peak value	Difference in breath hydrogen concentration (BHC, ppm) in probiotic group compared to placebo, measured by breath hydrogen peak value	During the 6-hour acute lactose challenge
Secondary	Difference in breath hydrogen concentration (BHC, ppm) in lactase group compared to placebo, measured by cumulative breath hydrogen value	Difference in breath hydrogen concentration (BHC, ppm) in lactase group compared to placebo, measured by cumulative breath hydrogen value	During the 6-hour acute lactose challenge
Secondary	Difference in breath hydrogen concentration (BHC, ppm) in probiotic group compared to placebo, measured by cumulative breath hydrogen value	Difference in breath hydrogen concentration (BHC, ppm) in probiotic group compared to placebo, measured by cumulative breath hydrogen value	During the 6-hour acute lactose challenge
Secondary	Difference in the severity of abdominal pain in lactase group compared to placebo, as defined by the gastrointestinal symptom survey	Difference in the severity of abdominal pain in lactase group compared to placebo, as defined by the gastrointestinal symptom survey	During the 6-hour acute lactose challenge
Secondary	Difference in the severity of abdominal pain in probiotic group compared to placebo, as defined by the gastrointestinal symptom survey	Difference in the severity of abdominal pain in probioticgroup compared to placebo, as defined by the gastrointestinal symptom survey	During the 6-hour acute lactose challenge
Secondary	Difference in the severity of flatulence in lactase group compared to placebo, as defined by the gastrointestinal symptom survey	Difference in the severity of flatulence in lactase group compared to placebo, as defined by the gastrointestinal symptom survey	During the 6-hour acute lactose challenge
Secondary	Difference in the severity of flatulence in probiotic group compared to placebo, as defined by the gastrointestinal symptom survey	Difference in the severity of flatulence in probiotic group compared to placebo, as defined by the gastrointestinal symptom survey	During the 6-hour acute lactose challenge
Secondary	Difference in the severity of bloating in lactase group compared to placebo, as defined by the gastrointestinal symptom survey	Difference in the severity of bloating in lactase group compared to placebo, as defined by the gastrointestinal symptom survey	During the 6-hour acute lactose challenge
Secondary	Difference in the severity of bloating in probiotic group compared to placebo, as defined by the gastrointestinal symptom survey	Difference in the severity of bloating in probiotic group compared to placebo, as defined by the gastrointestinal symptom survey	During the 6-hour acute lactose challenge
Secondary	Difference in the severity of nausea in lactase group compared to placebo, as defined by the gastrointestinal symptom survey	Difference in the severity of nausea in lactase group compared to placebo, as defined by the gastrointestinal symptom survey	During the 6-hour acute lactose challenge
Secondary	Difference in the severity of nausea in probioticgroup compared to placebo, as defined by the gastrointestinal symptom survey	Difference in the severity of nausea in probiotic group compared to placebo, as defined by the gastrointestinal symptom survey	During the 6-hour acute lactose challenge
Secondary	Difference in the presence of vomiting in lactase group compared to placebo, as defined by the gastrointestinal symptom survey	Difference in the presence of vomiting in lactase group compared to placebo, as defined by the gastrointestinal symptom survey	During the 6-hour acute lactose challenge
Secondary	Difference in the presence of vomiting in probiotic group compared to placebo, as defined by the gastrointestinal symptom survey	Difference in the presence of vomiting in probiotic group compared to placebo, as defined by the gastrointestinal symptom survey	During the 6-hour acute lactose challenge
Secondary	Difference in the presence of bowel movements in lactase group compared to placebo, as defined by the gastrointestinal symptom survey	Difference in the presence of bowel movements in lactase group compared to placebo, as defined by the gastrointestinal symptom survey	During the 6-hour acute lactose challenge
Secondary	Difference in the presence of bowel movements in probiotic group compared to placebo, as defined by the gastrointestinal symptom survey	Difference in the presence of bowel movements in probiotic group compared to placebo, as defined by the gastrointestinal symptom survey	During the 6-hour acute lactose challenge
Secondary	Difference in the presence of diarrhea in lactase group compared to placebo, as defined by the gastrointestinal symptom survey	Difference in the presence of diarrhea in lactase group compared to placebo, as defined by the gastrointestinal symptom survey	During the 6-hour acute lactose challenge
Secondary	Difference in the presence of diarrhea in probiotic group compared to placebo, as defined by the gastrointestinal symptom survey	Difference in the presence of diarrhea in probiotic group compared to placebo, as defined by the gastrointestinal symptom survey	During the 6-hour acute lactose challenge