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Clinical Trial Summary

The present study is a randomized, placebo-controlled, double-blind, parallel group study to assess the gut health effects of IP as compared to a placebo in overweight individuals experiencing gut issues. Approximately 20 participants aged between 18 and 65 years will be screened for each group. All the five arms of the IP and placebo trial arms will each have at least 10 completed participants after accounting for the screening failure and dropout/withdrawal rate of 20% each. The treatment duration for all the study participants will be 29 days.


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms


NCT number NCT05952232
Study type Interventional
Source Vedic Lifesciences Pvt. Ltd.
Contact Dr. Shalini Srivastava, MBBS, MD
Phone 42172300
Email shalini.s@vediclifesciences.com
Status Recruiting
Phase N/A
Start date August 17, 2023
Completion date April 15, 2024

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