U.S., Feb. 6 -- ClinicalTrials.gov registry received information related to the study (NCT06808867) titled 'Efficacy of Dietary Supplement in Subjects With Acid Reflux and/or Abdominal Bloating/Distention and GI Symptoms' on Jan. 30.
Brief Summary: This study was a prospective randomized clinical study. There was interventional treatment for a total of 8 weeks including a 2-week washout period. The subjects attended four appointments in the clinic throughout the duration of the study.
Study Primary Objective:
* To assess improvement in bloating symptoms
Study Secondary Objectives:
* To assess safety and tolerability of the formulation
* To compare the time taken for perceptual improvement in bloating/distention
* Enzyme blood assays...