None listed
Conditions
Interventions
Sponsors
Eligibility
Inclusion criteria
Inclusion criteria: Healthy males aged 18 to 55 years Body mass index BMI 18.5 to 29.9 kg/m Ability to understand the risks or benefits of the protocol. Normal baseline testosterone levels as per laboratory reference range. Willing to abstain from other supplements or medications that may affect study outcomes. Able and willing to provide written informed consent.
Exclusion criteria
Exclusion criteria: History or evidence of endocrine disorders or hypogonadism. Use of anabolic steroids, testosterone therapy, or hormone altering supplements within 3 months. Chronic illness example, diabetes, cardiovascular, renal, hepatic disease. Known allergy or hypersensitivity to any component of the investigational product. Participation in another clinical trial within the past 3 months. Substance abuse or alcohol dependence. Any condition that, in the investigator s opinion, may interfere with study compliance or data interpretation.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| To evaluate the effect of the testosterone booster supplement on total serum testosterone levels at specified time points in healthy male adults.Timepoint: Visit1 and Visit 3. | — |
Secondary
| Measure | Time frame |
|---|---|
| To assess the effect of supplementation on muscle endurance - Cooper test.Timepoint: Visit1 and Visit 3. | — |
Countries
India
Contacts
Unitree Health Care Diagnostics