Trials / Completed
CompletedNCT05599282
The Efficacy and Safety of an Amino Acid Supplement in Adults
A 90-day, Double-blind, Placebo-controlled, Randomized, Parallel-Group Efficacy and Safety Study of an Amino Acid Supplement in Adults
- Status
- Completed
- Phase
- Phase 2
- Study type
- Interventional
- Enrollment
- 120 (actual)
- Sponsor
- ZandA Technologies, llc · Academic / Other
- Sex
- All
- Age
- 35 Years – 75 Years
- Healthy volunteers
- Accepted
Summary
The primary objective of this clinical trial is to determine the efficacy of once daily oral AAS use, as compared to placebo, in increasing serum IGF-1 concentrations within adults aged 35-75 years for up to 90 days. Additionally, the safety and tolerability of the AAS, as compared to placebo, will be measured by the occurrence of and/or changes in treatment-emergent adverse events (AEs). For the study population, the eligibility criteria limit the presence of confounding variables that could influence study outcomes. Participants will be men and women between 35 and 75 years of age to account for the age range in which humans experience a decline in HGH/IGF-1. Each participant will be deemed eligible to participate by the Qualified Investigator (QI) by means of an extensive review of medical history, laboratory results, and physical examination. Participants will be required to have body mass index (BMI) measurements between 18.5 and 35.0 kg/m2 to ensure that their body weight/composition will not have a confounding effect on their HGH levels (18, 19) and to facilitate generalizability. Participants will be required to maintain current medication and supplements use and sleep throughout the study. They must also abstain from any over-the counter (OTC) medications and/or supplements that may affect the efficacy or safety of the AAS.
Conditions
Interventions
| Type | Name | Description |
|---|---|---|
| DRUG | Amino Acid Supplement | Four capsules of Amino Acid Supplement will be taken once a day for 90 days. |
| OTHER | Placebo | Four capsules of Placebo will be taken once a day for 90 days. |
Timeline
- Start date
- 2022-10-26
- Primary completion
- 2024-01-08
- Completion
- 2024-01-22
- First posted
- 2022-10-31
- Last updated
- 2024-04-04
Locations
1 site across 1 country: Canada
Source: ClinicalTrials.gov record NCT05599282. Inclusion in this directory is not an endorsement.