Clinical Trials Directory

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

TypeNameDescription
DIETARY_SUPPLEMENTSalvia haenkei 175mgThe product appears as a soft gel containing the dry extract of Salvia haenkei
DIETARY_SUPPLEMENTSalvia haenkei 350mgThe 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.