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
| Type | Name | Description |
|---|---|---|
| OTHER | Aqueous extract of roots plus leaves of Withania somnifera 125 mg | One capsule before breakfast for 84 days |
| OTHER | Aqueous extract of roots plus leaves of Withania somnifera 250 mg | One capsule before breakfast for 84 days |
| OTHER | Microcrystalline Cellulose | One 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.