Incidence of Lactose Intolerance Among Self-reported Lactose Intolerant People

Lactose Intolerance Clinical Trial

Official title:

Incidence of Lactose Intolerance Among Self-reported Lactose Intolerant People

Clinical Trial Details — Status: Completed

Administrative data

• NCT number: NCT02878876
• Other study ID #: 15-SC-11-A2-004
• Status: Completed
• Phase: Phase 4
• First received: August 16, 2016
• Last updated: August 22, 2016
• Start date: January 2016
• Est. completion date: March 2016

Study information

• Verified date: August 2016
• Source: a2 Milk Company Ltd.
• Contact: n/a
• Is FDA regulated: No
• Health authority: China: Ethics Committee
• Study type: Interventional

Clinical Trial Summary

This is a 3-sites, double-blinded, randomized, 2X2 cross-over study aiming to compare effects of milk containing only A2 type beta casein versus milk containing both A1 and A2 beta casein proteins on the gastrointestinal symptoms for the health people who self-reported to be lactose intolerant.

Description:

Study sites: Shanghai, Guangzhou, Beijing

Eligible subjects were enrolled in the study and randomized into one of the 2 study arms:

Sequence A1-A2: Oral consumption of milk containing both A1 and A2 type beta casein at Visit 1 and milk containing only A2 type beta casein at Visit 2; Sequence A2-A1: Oral consumption of milk containing only A2 type beta casein at Visit 1 and milk containing both A1 and A2 type beta casein at Visit 2.

Washout period: 2 weeks between Visit 1 and Visit 2

Recruitment information / eligibility

• Status: Completed
• Enrollment: 600
• Est. completion date: March 2016
• Est. primary completion date: March 2016
• Accepts healthy volunteers: Accepts Healthy Volunteers
• Gender: Both
• Age group: 20 Years to 50 Years

Eligibility

Inclusion Criteria:

• 20~50 years old male or female subjects;

• Non-regular milk drinker with self-reported intolerance to commercial milk;

• Suffered from mild to moderate digestive discomfort after milk consumption;

• Have normal electrocardiograms (ECG) and blood pressure during quiet respiration;

• Agree not to take any medication, supplements, nutrition or other dairy products including acidophilus milk;

• Be willing to comply with all the requirements and procedures of the study;

• Agree to sign the informed consent form;

• Agree not to enroll in another interventional clinical research study while participating in this study;

• Fully understand the nature, objective, benefit and the potential risks and side effects of the study.

Exclusion Criteria:

• Female on pregnant or feeding;

• Have known dairy allergy;

• Have severe response to milk intolerance;

• Have history of faecal impaction;

• Trying to lose weight by following a diet or exercise regimen designed for weight loss, or taking any drug influencing appetite and any drug for weight loss for the last three months ;

• Have participated in similar dairy or probiotics-containing product's clinical trials within 3 months before the screening;

• Currently taking medicines for cardiovascular or metabolic disease;

• Have history of or be diagnosed of any of the following diseases that may affect the study results: gastrointestinal disorders, hepatopathy, nephropathy, endocrine disease, blood disorders, respiratory and cardiovascular diseases;

• Current or previous alcohol abuser, currently taking or took illicit drugs, substance or OTC prescription drugs in regular frequency which may affect gastrointestinal disorders and study result;

• Currently suffering from any gastrointestinal disorders or gastrointestinal disease, including but not limited to: irritable bowel syndrome, colitis, ulcerative colitis, celiac disease, irritable bowel syndrome(IBS);

• Had hospitalizations within 3 months before screening;

• Currently drug frequency user of that may affect the gastrointestinal function or immune system. As judged by investigator.

Study Design

Allocation: Randomized, Endpoint Classification: Efficacy Study, Intervention Model: Crossover Assignment, Masking: Double Blind (Subject, Investigator, Outcomes Assessor), Primary Purpose: Basic Science

Related Conditions & MeSH terms

• Lactose Intolerance

Intervention

Dietary Supplement:
• Oral consumption of milk with sequence A1-A2
Oral consumption of 300 ml of milk containing both A1 and A2 type beta casein at 8:00 a.m. on Visit 1 (after 12-hour fasting) and 300 ml of milk containing only A2 type beta casein at 8:00 a.m. on Visit 2 (after 12-hour fasting).
• Oral consumption of milk with sequence A2-A1
Oral consumption of 300 ml of milk containing only A2 type beta casein at 8:00 a.m. on Visit 1 (after 12-hour fasting) and 300 ml of milk containing both A1 and A2 type beta casein at 8:00 a.m. on Visit 2 (after 12-hour fasting).

Locations

Country	Name	City	State
n/a

Sponsors (1)

Lead Sponsor	Collaborator
a2 Milk Company Ltd.

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Gastrointestinal Symptom VAS scores at 3 hours	Gastrointestinal symptoms were self-measured by study subjects on a scale from 0 (not at all) to 9 (severe) at 3 hours after product consumption at Visit 1 and Visit 2. Data was analyzed as a repeated measures design using a mixed effects ANOVA with symptom VAS scores at 3-hour as outcome, study product (A1 or A2) and study visit (1 or 2) as fixed effects, and a random subject effect nested within the sequence of study treatment (A1-A2 or A2-A1) , and adjusted for baseline symptom scores. Type III tests of fixed effects were used for testing the effect of study products. Contrast tests were generated to compare means for each product.	Three hours after product intervention at each of Visit 1 and Visit 2	No
Secondary	The percentage of improvement in gastrointestinal symptoms after drinking A2 versus A1	The improvement in gastrointestinal symptoms after drinking A2 versus A1 were classified into 4 mutually exclusive categories according to the following definition: No symptom: have no gastrointestinal symptoms after drinking product A2 while having symptoms after drinking product A1.; Significant improvement: still have gastrointestinal symptom after drinking product A2, the reduction of symptom scores >3; Slight improvement: still have gastrointestinal symptom after drinking product A2, 1<=reduction of symptom scores<=3; No difference (not improved or worsen): reduction of symptom scores<=0; The frequency and percentage in each category of improvement for each single gastrointestinal symptom, as well as that for all symptoms, are summarized.	1 hour and 3 hours after product intervention	No
Secondary	Urinary galactose concentration	Urinary galactose (U-gal) concentration was measured at baseline and 3-hour of each of Visit 1 and Visit 2. Data was analyzed as a repeated measures design using a mixed effects ANOVA with fixed effects of study product (A1 or A2) and study visit (1 or 2) and a random subject effect nested within the sequence of study treatment (A1-A2 or A2-A1) , and adjusted for baseline symptom scores. Type III tests of fixed effects were used for testing the effect of study products. Contrast tests were generated to compare means for each product.; The U-gal measurements over the whole study period (both Visit 1 and Visit 2) for all subjects were also summarized by study product. Product difference was evaluated using one-way ANOVA.	baseline and 3 hours after product intervention of each of Visit 1 and Visit 2	No
Secondary	Gastrointestinal Symptom VAS scores at 1 hour	Gastrointestinal symptoms were self-measured by study subjects on a scale from 0 (not at all) to 9 (severe) at 1 hour after product consumption at Visit 1 and Visit 2. Data was analyzed as a repeated measures design using a mixed effects ANOVA with symptom VAS scores at 1-hour as outcome, study product (A1 or A2) and study visit (1 or 2) as fixed effects, and a random subject effect nested within the sequence of study treatment (A1-A2 or A2-A1) , and adjusted for baseline symptom scores. Type III tests of fixed effects were used for testing the effect of study products. Contrast tests were generated to compare means for each product.	One hour after product intervention at each of Visit 1 and Visit 2	No
Secondary	Change of urinary galactose concentration from baseline at 3 hours <0.27 mmol/L (Yes/No)	Based on the results of urinary galactose test, subjects were classified as lactose malabsorbers if they had an increase in urinary galactose concentration of <0.27 mmol/L at 3 hours after oral consumption of 15g lactose (corresponding to 300 ml of product A1). And those with an increase in urinary galactose concentration of =0.27 mmol/L at 3-hour were classified as lactose absorbers.	3 hours after product intervention of each of Visit 1 and Visit 2	No