Clinical Trials Directory

Trials / Completed

CompletedNCT05931315

A Study to Assess the Efficacy of CaroRite™ on Psychological Well-being, Oxidative Stress and Quality of Life in Healthy Individuals

A Randomized, Double-blind, Placebo-controlled Study to Assess the Efficacy of CaroRite™ on Psychological Well-being, Oxidative Stress and Quality of Life in Healthy Individuals

Status
Completed
Phase
N/A
Study type
Interventional
Enrollment
78 (actual)
Sponsor
Vedic Lifesciences Pvt. Ltd. · Industry
Sex
All
Age
18 Years – 60 Years
Healthy volunteers
Accepted

Summary

The present study is a randomized, placebo-controlled, double-blind clinical study in which 94 individuals will be screened, and considering a screening failure rate of 20%, approximately 76 participants will be randomized in a ratio of 1:1 to receive either CaroRite™ or placebo and will be assigned a unique randomization code. Each group will have at least 30 completed participants after accounting for a dropout/withdrawal rate of 20%. The intervention duration for all the study participants is 90 days.

Conditions

Interventions

TypeNameDescription
DIETARY_SUPPLEMENTCaroRite™One capsule to be taken immediately post-dinner / with dinner
DIETARY_SUPPLEMENTPlaceboOne capsule to be taken immediately post-dinner / with dinner

Timeline

Start date
2023-08-22
Primary completion
2024-03-15
Completion
2024-03-15
First posted
2023-07-05
Last updated
2024-04-15

Locations

4 sites across 1 country: India

Source: ClinicalTrials.gov record NCT05931315. Inclusion in this directory is not an endorsement.