Evaluation of the treatment efficacy by incrementally increasing dosage of cow's milk on patients with lactose intolerance
Not Applicable
- Conditions
- actose Intolerance
- Registration Number
- JPRN-UMIN000023298
- Lead Sponsor
- Tokyo Women's Medical University Medical Center East
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Complete: follow-up complete
- Sex
- All
- Target Recruitment
- 47
Inclusion Criteria
Not provided
Exclusion Criteria
1.Patients with cow's milk allergy 2.Patients with Chronic digestive diseases, hematologic diseases, endocrine/metabolic diseases, and psycho-neurologic diseases 3.Pregnant or expected female patients 4.Other patients that the research director considers to be unsuitable in the study.
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Changes in severity of abdominal symptoms before and after the treatment (8 weeks maximum) by continuing incremental increase of cow's milk load for certain period.
- Secondary Outcome Measures
Name Time Method 1.Ratio of abdominal symptoms (such as psychogenic causes) in single blind comparative study on cow's milk and lactose-reduced milk 2.Ratio of true lactose intolerance from the result of lactose tolerance test 3.Changes in before and after the treatment listed below Lactose tolerance test and intestinal bacterial flora