RecruitingNot ApplicableNCT06967051

The Efficacy of a Smart Phone-based Test on Measuring Pupillary Light Reflex Alterations Following Cannabis Use Healthy in Adults

An Open Label Pilot Study Evaluating the Efficacy of a Smart Phone-based Test on Measuring Pupillary Light Reflex Alterations Following Cannabis Use Healthy in Adults


Sponsor

Sobereye Inc.

Enrollment

20 participants

Start Date

May 22, 2025

Study Type

INTERVENTIONAL

Conditions

Summary

The goal of this open label study is to evaluate the efficacy of smart phone-based test (SOBEREYE OPTOVERA) on measuring pupillary light reflex (PLR) alterations following cannabis use healthy in adults. The main question it aims to answer is: Can SOBEREYE OPTOVERA detect PLR alterations following cannabis consumption in healthy adults, in comparison to a pupillometer? Participants will be given two 5 mg capsules to be ingested for the 10 mg THC dose or five 5 mg capsules to be ingested for the 25 mg THC. Participants will be asked to complete PLR tests throughout the study day.


Eligibility

Min Age: 21 Years

Plain Language Summary

Simplified for easier understanding

This clinical trial is studying Pupillary Light Reflex (PLR) Test, Pupillometer, and others for people with cannabis intoxication and drug effects. The study is currently recruiting participants at 1 location.

This summary was AI-generated to explain the trial in plain language. It is not medical advice. Always discuss eligibility with your doctor before enrolling in a clinical trial.

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Interventions

DRUGTetrahydrocannabinol (10 mg)

10 mg of Tetrahydrocannabinol (THC) provided as a softgel capsule

DRUGTetrahydrocannabinol (25 mg)

25 mg of THC provided as a softgel capsule.

DIAGNOSTIC_TESTPupillary Light Reflex (PLR) Test

SOBEREYE OPTOVERA is a portable, non-invasive test that measures the Pupillary Light Reflex (PLR)

DIAGNOSTIC_TESTPupillometer

NeuroLight is an automated pupillometer that generates a flash of light and measures the photomotor reflex very accurately.


Locations(1)

KGK Science Inc.

London, Ontario, Canada

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NCT06967051


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