Phase
Condition
Ulcers
Gastrointestinal Diseases And Disorders
Treatment
Placebo
HMO 1
HMO 2
Clinical Study ID
Ages 40-55 All Genders Accepts Healthy Volunteers
Study Summary
Eligibility Criteria
Inclusion
Inclusion Criteria:
Age ≥ 40 and ≤ 55 years
Male/female
Total score of >2 on the Gastrointestinal Symptom Rating Scale (GSRS)
Body Mass Index 18-30 kg/m2
Stable body weight (± 5%) for at least 6 months
Stable lifestyle and dietary habits within the 4 weeks prior and during study period
Owns device (computer, smartphone, tablet) with access to the internet
Adequate fluency in the English language to understand the inform consent process,study instructions and study assessments
Sufficient vision and hearing to complete study procedures
Willing and able to participate, follow the study procedures and to give writteninformed consent
Exclusion
Exclusion Criteria:
History (< 6 months prior to the study) or presence of severe gastrointestinal,metabolic, immunological, psychiatric disorder, or major surgery
Current or past (< 4 weeks) use of prescription, over-the-counter, or traditionalmedication, or dietary supplements with a relevant impact on GI system or onvisceral motility
Having received antibiotic treatment < 4 weeks prior to study
Alcohol intake >1 units/day
Currently pregnant or pregnancy in past 6 months
Use of pro/prebiotics < 4 weeks prior to study start
Fully vegetarian/vegan diet < 4 weeks prior to study start
High habitual vegetable and fruit intake (> 2 servings of fruits and >2 servings ofvegetables per day) < 4 weeks prior to study start
Lactose intolerance
Maltodextrin allergy
Members of the research team or their immediate family members. Immediate familymember is defined as spouse, parent, child, or sibling, whether biological orlegally adopted
Study Design
Study Description
Connect with a study center
Singapore Institute for Clinical Trials
Singapore, 117609
SingaporeSite Not Available

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