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Clinical Trials/NCT04596644
NCT04596644
Suspended
Phase 2

Impact of Repeatedly-Administered THC-cannabis on Experimental Pain and Abuse Liability in Humans

New York State Psychiatric Institute1 site in 1 country16 target enrollmentAugust 1, 2021

Overview

Phase
Phase 2
Intervention
Active Cannabis
Conditions
Cannabis
Sponsor
New York State Psychiatric Institute
Enrollment
16
Locations
1
Primary Endpoint
Change in Cold Pressor Test (CPT) latency
Status
Suspended
Last Updated
7 months ago

Overview

Brief Summary

Chronic pain is a significant public health concern in the U.S., for which prescription opioids have historically been the standard treatment. This has resulted in striking rates of opioid use disorders and fatal overdoses. Identifying non-opioid medications for the management of chronic pain with minimal abuse liability is a public health necessity, and cannabinoids are a promising drug class for this purpose. More than 80% of medicinal cannabis users report pain as their primary medical indication, and they report experiencing minimal psychoactive effects. However, there are few well-controlled human laboratory studies assessing cannabis' efficacy for pain in the context of abuse, and even less is known regarding the effects of daily repeated use of cannabis on pain and its relationship to abuse liability. Carefully controlled research is needed.

The proposed randomized, within-subjects, placebo-controlled 16-day crossover inpatient human laboratory study (N = 20 healthy cannabis users; 10 men, 10 women) will address three important gaps in our understanding of the potential therapeutic utility of cannabis for pain: 1) Does tolerance develop to repeated, daily smoked cannabis administration on measures of experimental pain and abuse liability; 2) If so, is tolerance reversed during the 7 days of abstinence from active-THC cannabis; 3) Does abrupt abstinence from active cannabis increase experimental pain sensitivity, i.e. hyperalgesia, relative to baseline, and do these effects parallel measures of cannabis withdrawal such as disrupted mood and sleep?

Two distinct modalities of experimental pain will be assessed: The Cold Pressor Test (CPT) and Quantitative Sensory Testing Thermal Temporal Summation (QST-TTS). Throughout the study, experimental pain and abuse-related effects will be assessed, as will sleep and subjective mood assessments.

Registry
clinicaltrials.gov
Start Date
August 1, 2021
End Date
October 31, 2025
Last Updated
7 months ago
Study Type
Interventional
Study Design
Single Group
Sex
All

Investigators

Responsible Party
Principal Investigator
Principal Investigator

Caroline A. Arout, Ph.D.

Assistant Professor of Clinical Neurobiology (in Psychiatry)

New York State Psychiatric Institute

Eligibility Criteria

Inclusion Criteria

  • Males/non-pregnant females, 21-60 years old
  • Current cannabis user
  • Able to perform all study procedures

Exclusion Criteria

  • Use of other illicit drugs
  • If medical history, physical and psychiatric examination, or laboratory tests performed during the screening process reveal any significant illness that the study physician deems contraindicated for study participation
  • Insensitivity to the cold-water stimulus of the Cold Pressor Test or the heat stimulus of Quantitative Sensory Testing

Arms & Interventions

Dose A: Standardization Phase

On the first full inpatient day (Day 1), participants smoke one specified strength (Dose A; 75% of two 6.58% cannabis cigarettes) of cannabis at three timepoints.

Intervention: Active Cannabis

Dose B: Placebo Phase

On Days 2-8, participants smoke a second strength (Dose B; 75% of two \< 0.01%THC:CBD cannabis cigarettes) of cannabis will be administered 3x/day.

Intervention: Placebo Cannabis

Dose A: Active Phase

On Days 9-15, cannabis Dose A will be administered again (75% of two 6.58% cannabis cigarettes) at three timepoints each day.

Intervention: Active Cannabis

Outcomes

Primary Outcomes

Change in Cold Pressor Test (CPT) latency

Time Frame: Up to 15 days

The CPT apparatus consists of two refrigerated circulators, filled with warm (36.5-37.5°C). participants will complete the CPT 30 minutes before the 1000h cannabis administration (baseline), and 0, 15, 30, 45, 60, and 90 minutes post-cannabis administration. and cold (3.5 - 4.5°C) water. Participants will insert their non-dominant hand into the warm water and remove it after 3 minutes; skin temperature of the thumb pad will be measured. Participants will then insert their hand in the cold water and will be instructed to report when they first experience pain (pain threshold) and remove their hand when the cold water can no longer be tolerated (pain tolerance). Maximum immersion time will be 3 minutes. Repeats on days 1, 2, 5, 8, 9, 12, and 15.

Secondary Outcomes

  • Change in Quantitative Sensory Testing-Thermal Temporal Summation (QST-TTS) ratings(Up to 15 days)
  • Change in Cannabis Rating Form (CRF) ratings(Up to 15 days)

Study Sites (1)

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