Trials / Recruiting
RecruitingNCT07380412
A Study to Evaluate the Effects of a Supplement on the Side Effects Associated With Stimulant Medications
- Status
- Recruiting
- Phase
- N/A
- Study type
- Interventional
- Enrollment
- 90 (estimated)
- Sponsor
- Outliers, Inc. · Industry
- Sex
- All
- Age
- 18 Years – 55 Years
- Healthy volunteers
- Accepted
Summary
This is a hybrid, two-arm, triple-blind, placebo-controlled, randomized clinical trial evaluating the efficacy of the Stasis supplement on reducing oxidative stress, cortisol levels, and side effects associated with stimulant medications used for ADHD over a three-month period in adults.
Conditions
Interventions
| Type | Name | Description |
|---|---|---|
| DIETARY_SUPPLEMENT | Stasis Daytime and Nighttime | Daytime taken with stimulant medication and food. Nighttime taken 30 minutes before bedtime on an empty stomach. |
| DIETARY_SUPPLEMENT | Placebo | Matched placebo product in taste and appearance. |
Timeline
- Start date
- 2025-08-12
- Primary completion
- 2026-03-01
- Completion
- 2026-03-01
- First posted
- 2026-02-02
- Last updated
- 2026-02-02
Locations
1 site across 1 country: United States
Source: ClinicalTrials.gov record NCT07380412. Inclusion in this directory is not an endorsement.