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

Part of paid clinical trials in Las Vegas, Nevada.

Sponsor
Outliers, Inc.
Study ID
NCT07380412
Status
Recruiting

Conditions

  • ADHD
  • Brain Fog
  • Sleep Disturbance

Eligibility Criteria

Sex
ALL
Age
18 Years - 55 Years
Healthy Volunteers
Accepted

Interventions

  • Stasis Daytime and Nighttime — DIETARY_SUPPLEMENT
    Daytime taken with stimulant medication and food. Nighttime taken 30 minutes before bedtime on an empty stomach.
  • Placebo — DIETARY_SUPPLEMENT
    Matched placebo product in taste and appearance.

Study Details

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.

Key Dates

Start date
Aug 12, 2025
Status verified
Jan 2026
Primary completion
Mar 31, 2026
Completion
Mar 31, 2026

Study Design

Enrollment
90 participants (estimated)
Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT

Arms

  • Experimental: Stasis Supplement
  • Placebo Comparator: Placebo Comparator

Primary Outcome Measure

Change in oxidative stress and cortisol levels as measured by hs-CRP, 8-OHdG [ Time Frame: Baseline and Month 3 ]

Central Contacts

Locations (1)

FacilityCityStateZIPSite coordinators
CitruslabsLas VegasNevada89118
Patrick Renner, MSc
424-245-0284

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