Efficacy and Tolerability of Sensoril® in Improving Immunity and Thereby Reducing Incidence of Upper Respiratory Tract Infections

Immune Health Clinical Trial

Official title:
Efficacy and Tolerability of Sensoril® in Improving Immunity and Thereby Reducing Incidence of Upper Respiratory Tract Infections

Status Completed

Clinical Trial Summary

to assess the efficacy and safety of a standardized Withania somnifera extract (Sensoril®) as an immunomodulator in individuals suffering from recurrent URTIs. The study population will be administered with this unique blend of WS extract for 12 weeks and will be assessed as per the study designated efficacy and safety variables.

Clinical Trial Description

n/a

Study Design

Related Conditions & MeSH terms

Clinical Trial Details

NCT number	NCT04733924
Study type	Interventional
Source	Vedic Lifesciences Pvt. Ltd.
Contact
Status	Completed
Phase	N/A
Start date	January 21, 2021
Completion date	September 23, 2021

View Details

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