Stasis Supplement for Stimulant Side Effects in ADHD

This study is looking at whether a dietary supplement called Stasis Daytime and Nighttime can help reduce side effects from stimulant medications used for ADHD. These side effects include sleep difficulties, irritability, anxiety, and brain fog. Researchers will compare Stasis to a placebo (an inactive product that looks and tastes the same) over three months. They will measure changes in levels of oxidative stress and cortisol (a stress hormone) in your body. You might be able to join if you are 18-55 years old, currently take stimulant medication for ADHD, and experience these side effects. You also need to be a US resident and willing to keep your current habits.

Study design
This is a triple-blind, randomized study comparing two groups (Stasis vs. placebo) and plans to enroll 90 adults.
What's involved
You would take the Stasis Daytime supplement with your stimulant medication and food, and Stasis Nighttime 30 minutes before bed on an empty stomach for three months. Blood tests will be done at the start and after three months.
Compensation
Not stated in the trial record.
Follow-up
Your progress will be monitored for three months, with measurements taken at the beginning and end of this period.

AI-generated from the public study record. Only the study team can confirm whether you're eligible — confirm details with them before making decisions.

NCT07380412

A Study to Evaluate the Effects of a Supplement on the Side Effects Associated With Stimulant Medications

Recruiting
NAAges 18–55InterventionalTreatment
Outliers, Inc.
~90 participants
Updated 2026-02-02 on ClinicalTrials.gov
What's tested:Stasis Daytime and NighttimePlacebo

At a glance

Recruiting sites
1 of 1 listed site is recruiting right now
RecruitingSuspended, closed, or not yet open
What they're measuring
Change in oxidative stress and cortisol levels as measured by hs-CRP, 8-OHdG
Measured over Baseline and Month 3
+1 more outcome measured
ADHD
Sleep Disturbance
Brain Fog
1 sites across 1 states
Nevada1

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Eligibility criteria

Inclusion

Aged 18-55 years
Currently prescribed stimulant medication for ADHD
Experiencing: sleep difficulty, irritability, anxiety, brain fog
Stable medication dose ≥3 months
Healthy with no uncontrolled chronic conditions
Stable on supplements ≥3 months if applicable
US resident
Willing to maintain current habits

Exclusion

Chronic conditions (e.g. cancer, mental illness)
Use of psychiatric medications besides stimulants
Pregnancy, breastfeeding, thyroid, liver, kidney conditions
Recent smokers or heavy alcohol use
Night shift workers
Participation in other clinical trials
Allergies to product ingredients
  • Change in oxidative stress and cortisol levels as measured by hs-CRP, 8-OHdGBaseline and Month 3

    Measurement of oxidative stress and cortisol levels will be assessed using the following validated biomarkers: hs-CRP and serum cortisol from blood samples 8-hydroxy-2'-deoxyguanosine (8-OHdG) from urine samples

  • Change in cortisol levelsBaseline and Month 3

    Serum cortisol concentration measured via blood draw.