Effects of Dronabinol in Opioid Maintained Patients

Pain Clinical Trial

— THC  

Official title:

The Effects of Dronabinol in Opioid-Related Outcomes

Clinical Trial Details — Status: Recruiting

Administrative data

• NCT number: NCT04025359
• Other study ID #: 2000027065
• Status: Recruiting
• Phase: Early Phase 1
• Start date: May 31, 2019
• Est. completion date: December 30, 2024

Study information

• Verified date: May 2023
• Source: Yale University
• Contact: Joao De Aquino, M.D.
• Phone: 203-932-5711
• Email: joao.deaquino[@]va.gov
• Is FDA regulated: No
• Study type: Interventional

Clinical Trial Summary

Twenty male and female (ages 18-70) participants with OUD currently receiving methadone or buprenorphine will be enrolled. Prior to their daily methadone or buprenorphine dose and thus at trough plasma levels of opioid, participants will receive dronabinol (2.5 mg, 5mg) or placebo. Subsequently, all participants will undergo laboratory testing of opioid-related outcomes. Pain sensitivity will be measured using a technique called the (QST) quantitative sensory testing, which involves the administering heat or cold stimulation. A Short-Form McGill Pain Questionnaire (SF-MPQ) and a pain Visual Analog Scale (VAS). Attentional bias will be measured using a visual probe task. Negative affect will be measured using the Positive and Negative Affect Schedule (PANAS). Cognitive performance will be measured by a comprehensive cognitive battery. The order of study medication administration will be counterbalanced order to minimize carryover effects. On the initial screening day and at the end of medication treatment, blood will be drawn to determine serum cytokine levels. One week after the last study medication dose, a follow-up session will be conducted during which participants will undergo urine toxicology testing and a safety evaluation before final discharge from the study.

Description:

This is a double-blind, randomized, placebo-controlled cross-over human laboratory study. Participants will be asked to come to the testing site for a total of four times: one initial screening session (~ 3 hours) and three test days (~ 6 hours each) where study medication will be administered, separated by at least 72 hours to limit carryover effects for dronabinol administration. Twenty male and female participants with OUD on MAT will be asked to arrive at approximately the same time each morning, coordinating with attendance at their opioid maintenance clinic. Subjects will be asked to refrain from using alcoholic beverages and drugs during study participation. Urine screens and breathalyzer measurements will be done before the test sessions to check abstinence from drugs (e.g., cocaine, illicit opioids, benzodiazepines, barbiturates, and amphetamines) and alcohol respectively. Those who are non-compliant will be discharged from the study. To minimize nicotine and withdrawal effects on cognitive performance, subjects who smoke will be advised to continue smoking as usual. Since we will provide a standard breakfast, participants will be asked not to eat for two hour before they arrive for the test sessions. A study nurse will confirm with their respective program that participants did not receive either methadone or buprenorphine that morning, and will call the program when testing is complete to permit dispersal of that day's methadone or buprenorphine dose. On the initial screening day and at the end of medication treatment, blood will be drawn to determine serum cytokine levels. Participants will undergo a variety of cognitive and self-report measures, as well as assessments to confirm restraint from illicit drug use and lack of adverse effects of medication. Prior to their daily methadone or buprenorphine dose and thus at trough plasma levels of opioid, participants will receive dronabinol (10 mg, 20 mg) or placebo. Subsequently, all participants will undergo laboratory testing of measures relevant to vulnerability to relapse, including physiological, subjective and cognitive outcomes. The order of study medication administration will be counterbalanced order to minimize the impact of potential carryover effects between the sessions. To date: 27 subjects completed the approve protocol. Recently, this study was amended to reduce the study drug (dronabinol) to 2.5mg, 5mg, or placebo. This study is active with recruit continuing under the new doses.

Recruitment information / eligibility

• Status: Recruiting
• Enrollment: 36
• Est. completion date: December 30, 2024
• Est. primary completion date: October 30, 2024
• Accepts healthy volunteers: No
• Gender: All
• Age group: 18 Years to 70 Years

Eligibility

Inclusion Criteria:

• Cannabis use, with recent cannabis exposure confirmed by urine toxicology.

• Males and females, Veterans and non-Veterans, aged between 18 and 70.

• Diagnosed with OUD and currently enrolled in methadone or buprenorphine maintenance treatment.

• Capable of providing informed consent in English.

• Compliant in opioid maintenance treatment and on a stable dose for two weeks or longer.

• Not meeting DSM-5 criteria for substance use disorders other than OUD or tobacco use disorder within the last 12 months.

• No current medical problems deemed contraindicated for participation by principal investigator.

• For women, not pregnant as determined by pregnancy screening; not breast-feeding; using acceptable birth control methods.

Exclusion Criteria:

• Currently meeting DSM-5 criteria for cannabis use disorder (CUD).

• History of primary psychotic disorders or other current major psychiatric disorders deemed clinically unstable by the principal investigator.

• Serious medical or neurological illness or treatment for a medical disorder that could interfere with study participation as determined by principal investigator.

• Inability to complete neuropsychological tests.

• A physician will carefully evaluate participants for use of over-the-counter or prescription psychoactive drugs known to affect pain threshold or pain tolerance (including NSAIDS, serotonin-norepinephrine reuptake inhibitors (SNRIs), (e.g. venlafaxine, duloxetine), tricyclic antidepressants (e.g., nortriptyline, amitriptyline), anticonvulsant medications (e.g., topiramate, tegretol), benzodiazepines (e.g., alprazolam, diazepam), and other opioid drugs). Only subjects who are on stable doses of these medications, and whose dosing schedules allow participation in the study visits, will be enrolled. If possible, the morning dose will be administered after the study visit.

• Liver function tests (ALT or AST) greater than 3x normal.

• Contraindications for exposure to cold temperatures, such as Raynaud's phenomenon and hypertension.

• Allergy or serious adverse reaction to cannabis, dronabinol or other cannabinoids.

Related Conditions & MeSH terms

• Pain

Intervention

Drug:
• Dronabinol
Dronabinol 2.5 mg
• Dronabinol
Dronabinol 5 mg
• Placebo
Placebo

Locations

Country	Name	City	State
United States	VA Healthcare System	West Haven	Connecticut

Sponsors (2)

Lead Sponsor	Collaborator
Yale University	US Department of Veterans Affairs

Country where clinical trial is conducted

United States, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Pain sensitivity, measured by the Cold Pressor Test (CPT).	Pain threshold and pain tolerance, in seconds.	up to 6 hours
Primary	Pain sensitivity, measured by the Short form of the McGill Pain Questionnaire (SF-MPQ).	Subjective pain measured by the SF-MPQ. The SF-MPQ values range from 0 to 45, with higher values indicating greater pain sensitivity.	up to 6 hours
Secondary	Abuse potential, measured by the Drug Effects Questionnaire (DEQ).	The DEQ values range from 0-100, with higher values indicating more prominent subjective drug effects.	up to 6 hours
Secondary	Cognitive Performance, measured by the Continuous Performance Test (CPT)	Sustained attention and verbal learning measured by the CPT. The outcome for the CPT is the percent of correct responses, with a higher percentage indicating greater attention and working memory performance.	up to 6 hours
Secondary	Cognitive Performance, measured by the Hopkins Verbal Learning Test (HVLT).	Sustained attention and verbal learning measured by the HVLT. The outcome for the HVLT is the immediate total recall, ranging from 0-36, with higher values indicating greater verbal learning.	up to 6 hours