Stasis supplement to reduce stimulant medication side effects

Is this trial a fit for you?

A plain-English reading of the study's rules. Only the study team can confirm whether you qualify.

What this trial studies

This is a hybrid, two-arm, triple-blind, randomized, placebo-controlled trial comparing Stasis daytime and nighttime supplements to matching placebo over three months in adults aged 18–55 who are on a stable stimulant dose for ADHD. Participants complete both remote and in-person components at the Citruslabs site in Las Vegas, with biomarker collection and symptom questionnaires at baseline and follow-up visits. Key outcomes include changes in oxidative stress markers, salivary or serum cortisol, and patient-reported stimulant side effects such as sleep disturbance, irritability, anxiety, and cognitive fog. The trial excludes people with uncontrolled medical or psychiatric conditions, recent smokers, heavy alcohol users, and those taking other psychiatric medications.

Why it matters

Who can join: the full rules

Inclusion Criteria:

* 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 Criteria:

* 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

Where it's running

• Citruslabs
  Las Vegas, Nevada, United States Recruiting

Study contacts

• Study coordinator: Patrick Renner, MSc
• Email: hello@citruslabs.com
• Phone: 4242450284

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How to take part

1. Review the eligibility criteria above with your treating physician.
2. Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
3. Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.