Trials / Recruiting
RecruitingNCT05936346
Evaluation of Safety and Tolerability of Salvia Haenkei Extract As a Dietary Supplement Ingredient
Evaluation of Safety and Tolerability of Salvia Haenkei Extract As a Dietary Supplement Ingredient in a Healthy Population: a Randomized, Open Label, Parallel-arm, Two-dose Study
- Status
- Recruiting
- Phase
- N/A
- Study type
- Interventional
- Enrollment
- 50 (estimated)
- Sponsor
- IBSA Farmaceutici Italia Srl · Industry
- Sex
- All
- Age
- 55 Years – 65 Years
- Healthy volunteers
- Accepted
Summary
Evalution of the safety and tolerability of the oral administration of Salvia haenkei in a healthy population.
Detailed description
The aim of the study is to assess the safety and tolerability of the oral administration of Salvia haenkei in a healthy population. Furthermore, Salvia haenkei has been identified as a potential anti-senescence agent and may counteract aging and aging-associated disorders. In this scenario, the current study aims also at exploring the effects of this supplementation on muscular and other organ functions (kidney, liver, heart, etc.) and on systemic inflammation and metabolism.
Conditions
Interventions
| Type | Name | Description |
|---|---|---|
| DIETARY_SUPPLEMENT | Salvia haenkei 175mg | The product appears as a soft gel containing the dry extract of Salvia haenkei |
| DIETARY_SUPPLEMENT | Salvia haenkei 350mg | The product appears as a soft gel containing the dry extract of Salvia haenkei |
Timeline
- Start date
- 2023-07-17
- Primary completion
- 2025-04-30
- Completion
- 2025-04-30
- First posted
- 2023-07-07
- Last updated
- 2025-01-23
Locations
1 site across 1 country: Switzerland
Source: ClinicalTrials.gov record NCT05936346. Inclusion in this directory is not an endorsement.