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临床试验/NCT04596644
NCT04596644暂停2 期

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

New York State Psychiatric Institute2 个研究点 分布在 1 个国家目标入组 16 人开始时间: 2021年8月1日最近更新:
适应症
干预措施
相关药物

试验速览

阶段
2 期
状态
暂停
入组人数
16
试验地点
2
主要终点
Change in Cold Pressor Test (CPT) latency

研究概览

简要总结

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.

研究设计

研究类型
Interventional
分配方式
Non Randomized
干预模型
Single Group
主要目的
Basic Science
盲法
None

入排标准

年龄范围
21 Years 至 60 Years(Adult)
性别
All
接受健康志愿者

入选标准

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

排除标准

  • 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

研究组 & 干预措施

Dose A: Standardization Phase

Experimental

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.

干预措施: Active Cannabis (Drug)

Dose B: Placebo Phase

Placebo Comparator

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.

干预措施: Placebo Cannabis (Drug)

Dose A: Active Phase

Experimental

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

干预措施: Active Cannabis (Drug)

结局指标

主要结局

Change in Cold Pressor Test (CPT) latency

时间窗: 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.

次要结局

  • 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)

研究者

申办方类型
Other
责任方
Principal Investigator
主要研究者

Caroline A. Arout, Ph.D.

Assistant Professor of Clinical Neurobiology (in Psychiatry)

New York State Psychiatric Institute

研究点 (2)

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