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Trials / Completed

CompletedNCT04733924

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

Status
Completed
Phase
N/A
Study type
Interventional
Enrollment
77 (actual)
Sponsor
Vedic Lifesciences Pvt. Ltd. · Industry
Sex
All
Age
18 Years – 50 Years
Healthy volunteers
Not accepted

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.

Conditions

Interventions

TypeNameDescription
OTHERAqueous extract of roots plus leaves of Withania somnifera 125 mgOne capsule before breakfast for 84 days
OTHERAqueous extract of roots plus leaves of Withania somnifera 250 mgOne capsule before breakfast for 84 days
OTHERMicrocrystalline CelluloseOne capsule before breakfast for 84 days

Timeline

Start date
2021-01-21
Primary completion
2021-04-29
Completion
2021-09-23
First posted
2021-02-02
Last updated
2021-10-19

Locations

3 sites across 1 country: India

Source: ClinicalTrials.gov record NCT04733924. Inclusion in this directory is not an endorsement.

Efficacy and Tolerability of Sensoril® in Improving Immunity and Thereby Reducing Incidence of Upper Respiratory Tract I (NCT04733924) · Clinical Trials Directory