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NCT07380412 · ClinicalTrials.gov registry record · NA
A Study to Evaluate the Effects of a Supplement on the Side Effects Associated With Stimulant Medications
A NA study of ADHD and Sleep Disturbance, sponsored by Outliers.
- Recruiting
- Registry status
- NA
- Development phase
- 90
- Enrollment target
- 1
- Study location
NCT07380412 is a NA study of ADHD and Sleep Disturbance that is actively recruiting participants, run by Outliers. The registered enrollment target is 90 participants, below the 189-participant average among 75 other ADHD trials with a reported enrollment target (52% lower). The trial reports 1 study location across 1 state.
The verdict
NCT07380412, a NA study of ADHD and Sleep Disturbance, is actively recruiting participants, sponsored by Outliers.
- RECRUITING
- Registry status
- NA
- Development phase
- 90 participants
- Enrollment target
- 1
- Study location
Study 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 Studied
Interventions
- DIETARY_SUPPLEMENT Placebo
- DIETARY_SUPPLEMENT Stasis Daytime and Nighttime
Study Locations (1)
Nevada
- Citruslabs - Las Vegas
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 90 participants |
| Start Date | 2025-08-12 |
| Est. Completion | 2026-03 |
| Phase | NA |
Interested in This Trial?
Full Details on ClinicalTrials.gov ↗What the Registry Record Tells You About NCT07380412
The ClinicalTrials.gov registry entry for NCT07380412 describes a study currently listed as recruiting, categorized as NA. The registered enrollment target is 90 participants, a figure that helps gauge the scale of data the investigators plan to collect, below the 189-participant average among 75 other ADHD trials with a reported enrollment target (52% lower). The listed sponsor is Outliers, which has 1 total studies on file at ClinicalTrials.gov.
The record links to 3 conditions, with ADHD appearing as the primary indexed condition, and to 2 interventions - of which Placebo is the first listed.
NCT07380412 reports 1 study location spanning 1 distinct geographic area - top geographies include Nevada.
Frequently Asked Questions
What is clinical trial NCT07380412 about?
NCT07380412 is a clinical study titled "A Study to Evaluate the Effects of a Supplement on the Side Effects Associated With Stimulant Medications". 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.
What is the current status of trial NCT07380412?
This trial is currently recruiting. It is a NA study. The enrollment target is 90 participants. The study started on 2025-08-12. Estimated completion is 2026-03.
What conditions does trial NCT07380412 study?
This clinical trial studies the following conditions: ADHD, Sleep Disturbance, Brain Fog.
What interventions are being tested in trial NCT07380412?
The interventions under investigation include: Placebo (DIETARY_SUPPLEMENT), Stasis Daytime and Nighttime (DIETARY_SUPPLEMENT).
Who is sponsoring clinical trial NCT07380412?
This trial is sponsored by Outliers, which has 1 total clinical trials registered on ClinicalTrials.gov.
Where is trial NCT07380412 being conducted?
This trial has 1 study location across Nevada. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.
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Read our methodology - how this data is sourced, computed, and verified.
Related
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