Stasis Supplement for ADHD
What You Need to Know Before You Apply
What is the purpose of this trial?
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.
Are You a Good Fit for This Trial?
Adults aged 18-55 with ADHD who are on a stable dose of stimulant medication for at least 3 months can join. They should be healthy, without uncontrolled chronic conditions, and have been stable on supplements if taking any. Participants must live in the US and agree to keep their current lifestyle habits during the trial.Inclusion Criteria
Timeline for a Trial Participant
Screening
Participants are screened for eligibility to participate in the trial
Treatment
Participants receive the Stasis supplement or placebo to evaluate its effects on oxidative stress, cortisol levels, and side effects associated with stimulant medications over a three-month period
Follow-up
Participants are monitored for safety and effectiveness after treatment
What Are the Treatments Tested in This Trial?
Interventions
- Stasis Daytime and Nighttime
Trial Overview
The study is testing 'Stasis Daytime and Nighttime' supplements against a placebo to see if they reduce side effects from ADHD stimulant medications. It's a three-month test where participants won't know which treatment they're getting, nor will the researchers initially.
How Is the Trial Designed?
2
Treatment groups
Experimental Treatment
Placebo Group
Find a Clinic Near You
Who Is Running the Clinical Trial?
Outliers, Inc.
Lead Sponsor
Citruslabs
Industry Sponsor
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