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NCT05952232

A Study to Evaluate Efficacy of Different Natural Ingredients in Improving Gut Health in Adults With Leaky Gut.

Completed NA Last updated 17 June 2024
What this trial tests

NA trial testing PA-GH-01 in Gut Health in 45 participants. Completed in 27 May 2024.

Timeline
17 August 2023
Primary endpoint
27 May 2024
27 May 2024

Quick facts

Lead sponsorVedic Lifesciences Pvt. Ltd.
PhaseNA
StatusCompleted
Study typeINTERVENTIONAL
Allocationrandomized
Designparallel
Maskingtriple
Primary purposeother
Enrollment45
Start date17 August 2023
Primary completion27 May 2024
Estimated completion27 May 2024
Sites2 locations across India

Drugs / interventions tested

Conditions studied

Sponsor

Vedic Lifesciences Pvt. Ltd. — full company profile →

Who can join

Adults 18 to 65, any sex, with Gut Health. Patients with the condition only — healthy volunteers not accepted.

Sponsor's own description

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.

Publications & conference data

No peer-reviewed publications indexed yet for this trial. Completed trials usually publish results within 12-18 months.

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Other recruiting trials for Gut Health

Currently open trials in the same condition.

Other Vedic Lifesciences Pvt. Ltd. trials

Trials by the same sponsor.

Verify against primary sources

Data sources for this page

Drug Landscape aggregates and links these public records for informational use only. Always verify against the primary source before clinical or regulatory decisions. Canonical URL: https://druglandscape.com/trial/NCT05952232.

Primary sources · FDA · ClinicalTrials.gov · EMA · SEC EDGAR · ChEMBL · Wikidata · full sourcing