Comparative Pharmacokinetic and Pharmacodynamic Effects of Delta-8 and Delta-9 THC

NCT05287256 · Status: COMPLETED · Phase: PHASE1 · Type: INTERVENTIONAL · Enrollment: 28

Last updated 2026-02-17

No results posted yet for this study

Summary

The current study will investigate the subjective, physiological, and cognitive performance effects of inhaled and orally ingested Delta-8 tetrahydrocannabinol (THC) in comparison to both placebo and Delta-9 THC. The purpose of this study is to assess the effects of Delta-8 THC as compared to placebo and Delta-9 THC. Oral fluid, urine, blood, and hair specimens will be collected from participants.

Conditions

  • Behavioral Pharmacology of Cannabis

Interventions

DRUG

Oral Delta-8-THC Cannabis

Delta-8-THC cannabis will be orally self-administered by study participants

DRUG

Oral Delta-9-THC Cannabis

Delta-9-THC cannabis will be orally self-administered by study participants

DRUG

Oral Placebo

Placebo will be orally self-administered by study participants

DRUG

Vaporized Delta-8-THC Cannabis

Delta-8-THC cannabis will be self-administered by study participants using a vaporizer

DRUG

Vaporized Delta-9-THC Cannabis

Delta-9-THC cannabis will be self-administered by study participants using a vaporizer

DRUG

Vaporized Placebo

Placebo will be self-administered by study participants using a vaporizer

Sponsors & Collaborators

  • Substance Abuse and Mental Health Services Administration (SAMHSA)

    collaborator FED
  • Johns Hopkins University

    lead OTHER

Principal Investigators

  • Ryan Vandrey, PhD · Johns Hopkins University

Study Design

Allocation
RANDOMIZED
Purpose
BASIC_SCIENCE
Masking
DOUBLE
Model
CROSSOVER

Eligibility

Min Age
18 Years
Max Age
45 Years
Sex
ALL
Healthy Volunteers
Yes

Timeline & Regulatory

Start
2022-05-23
Primary Completion
2024-08-08
Completion
2024-10-02
FDA Drug
Yes

Countries

  • United States

Study Locations

More Related Trials

Entities

Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT05287256 on ClinicalTrials.gov