Actively Recruiting

Phase Not Applicable
Age: 18Years - 55Years
All Genders
Healthy Volunteers
NCT07380412

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

Led by Outliers, Inc. · Updated on 2026-02-02

90

Participants Needed

1

Research Sites

28 weeks

Total Duration

On this page

Sponsors

O

Outliers, Inc.

Lead Sponsor

C

Citruslabs

Collaborating Sponsor

AI-Summary

What this Trial Is About

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

Official Title

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

Who Can Participate

Age: 18Years - 55Years
All Genders
Healthy Volunteers

Eligibility Criteria

Eligible

You may qualify if you...

  • Aged 18-55 years
  • Currently prescribed stimulant medication for ADHD
  • Experiencing sleep difficulty, irritability, anxiety, or brain fog
  • Stable medication dose for 3 months or more
  • Healthy with no uncontrolled chronic conditions
  • Stable on supplements for 3 months or more if applicable
  • US resident
  • Willing to maintain current habits
Not Eligible

You will not qualify if you...

  • Chronic conditions such as cancer or mental illness
  • Use of psychiatric medications other than stimulants
  • Pregnancy or breastfeeding
  • Thyroid, liver, or kidney conditions
  • Recent smoking or heavy alcohol use
  • Night shift workers
  • Participation in other clinical trials
  • Allergies to product ingredients

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Trial Site Locations

Total: 1 location

1

Citruslabs

Las Vegas, Nevada, United States, 89118

Actively Recruiting

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Research Team

P

Patrick Renner, MSc

CONTACT

How is the study designed?

Study Type

INTERVENTIONAL

Masking

TRIPLE

Allocation

RANDOMIZED

Model

PARALLEL

Primary Purpose

TREATMENT

Number of Arms

2

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