Randomized, Double-Blind, Placebo-Controlled, Single-Center Clinical Study, where participants will take the Daily Supplement, and record Daily Symptoms, two clinical visits where Hydrogen and Methane Breath Test (HMBT) will be conducted, Abdominal Circumference Measurement will be taken, and two Self Reported Validated Questionnaires: Visual Analogue Scale (VAS) and the Quality of Life Questionnaires.
Study Type
INTERVENTIONAL
Allocation
RANDOMIZED
Purpose
SUPPORTIVE_CARE
Masking
DOUBLE
Enrollment
50
Placebo
Dietary Supplement containing blend of Digestive Enzymes, Dandelion, Ginger \& Fennel Extracts
MusB Research
New Port Richey, Florida, United States
To determine the impact of BTB on hydrogen and methane production in healthy adults
Participants will take the Hydrogen and Methane Breath Test (HMBT) at baseline and after the study at Week4.
Time frame: From time of enrollement to end of study at Week4
To estimate the changes in abdominal circumference as an indicator of distention
Standardized tape measurement at the level of the iliac crest or on top of belly button will be used to evaluate changes in abdominal distention at baseline and after the study at Week4.
Time frame: From time of enrollement to end of study at Week4
To assess the changes in validated subjective questionnaire (VAS) for bloating, abdominal pain, distension, and flatulence.
Participants will take Visual Analogue Scale (VAS) which is a self-reported assessment of bloating and distention severity using PROMIS's GI gas and bloating questionnaire at baseline and after the study at Week4.
Time frame: From time of enrollement to end of study at Week4
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