Clinical Research Directory

A Study to Evaluate Acute and Short-term Efficacy of Digest Gold on Postprandial Abdominal Distension and Subjective Bloating in Healthy Adults

The goal of this clinical trial is to investigate the acute and short-term efficacy of Digest Gold on postprandial abdominal distension and subjective bloating in healthy adults. The main question it aims to answer is what is the difference between Digest Gold and placebo in time-to-relief of subjective bloating (time = 0 -120 minutes postprandial), as assessed by the bloating Likert scale?Researchers will compare Digest Gold to a placebo to see its effects on postprandial abdominal distension and bloating. Participants will: * Consume Digest Gold and a placebo. * Have height, weight, and waist circumference measured. * Have blood pressure and heart rate measured. * Provide blood samples. * Provide a fecal sample. * Complete study questionnaires assessing gastrointestinal symptoms and subjective bloating. * Record their daily food intake. * Complete a breath test to assess gastrointestinal parameters.