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Clinical Trial Summary

This is a randomized, double-blind, placebo-controlled, 3 arm parallel group study of 12 weeks duration, with a 4-week run-in period as the control phase and an 8-week intervention period, to investigate the effectiveness of the treatment on upper GI disturbance.


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms


NCT number NCT06104917
Study type Interventional
Source RDC Clinical Pty Ltd
Contact Amanda Rao, PhD
Phone +61 414 488 559
Email amanda@rdcglobal.com.au
Status Recruiting
Phase Phase 3
Start date February 21, 2024
Completion date February 28, 2025

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