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Effect of Cannabis and Endocannabinoids on HIV Neuropathic Pain

Primary Purpose

Cannabis, HIV Neuropathy, Pain Syndrome

Status
Completed
Phase
Phase 2
Locations
United States
Study Type
Interventional
Intervention
Cannabis
Sponsored by
University of California, San Diego
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Cannabis focused on measuring neuropathic pain, human immunovirus, vaporized cannabis

Eligibility Criteria

18 Years - undefined (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  1. the ability to provide informed consent
  2. age 18 or older
  3. HIV infection documented at the HNRP or assessed by an HIV test at screening;
  4. a diagnosis of HIV sensory neuropathy
  5. current use of cannabis
  6. the ability to describe the THC and CBD content in the products they use, i.e., obtaining cannabis from dispensaries that list THC and CBD content
  7. ability to respond to daily text message

Exclusion Criteria:

  1. meeting criteria for current substance or alcohol dependence
  2. traumatic brain injury
  3. dementia or Alzheimer's disease
  4. psychosis
  5. a respiratory condition, i.e., pulmonary disease, that would be exacerbated by inhaling vaporized cannabis
  6. history of cardiovascular disease, including myocardial infarction or stroke;
  7. uncontrolled hypertension, defined as a systolic blood pressure greater than 160 mm Hg or a diastolic blood pressure greater than 100 mm Hg
  8. pregnancy, breastfeeding, or unwillingness to prevent pregnancy during the cannabis administration portion of the study (using birth control in female participants of child- bearing age)
  9. unwillingness or inability to receive or respond to text messages

Sites / Locations

  • UC Center for Medicinal Cannabis Research, UC San Diego

Arms of the Study

Arm 1

Arm 2

Arm 3

Arm Type

Active Comparator

Active Comparator

Active Comparator

Arm Label

Low CBD session

Medium CBD session

High CBD session

Arm Description

In the morning, participants will inhale 8 puffs of vaporized cannabis containing 1.6% THC + 0.09 CBD. They will then undergo experimental testing as described below under Outcome Measures.

In the morning, participants will inhale 8 puffs of vaporized cannabis 4 puffs will contain 1.6% THC + 0.09 CBD and 4 puffs will contain 1.73% THC + 5.4% CBD. They will then undergo experimental testing as described below under Outcome Measures.

In the morning, participants will inhale 8 puffs of vaporized cannabis containing 1.73% THC + 5.4% CBD. They will then undergo experimental testing as described below under Outcome Measures.

Outcomes

Primary Outcome Measures

Phase 1 - numerical 11-point Pain Intensity Scale
an ordinal scale
Phase 2 - numerical 11-point Pain Intensity Scale
participants receive interactive text questions sent once a day to their cell phone asking them to indicate their average pain level for the day on a 0 to 10 scale

Secondary Outcome Measures

Phase 1 - Patient Global Impression of Change (PGIC)
a 7 point ordinal scale reflective of improvement in pain
Phase 1 - von Frey test
The von Frey filament will be applied on the dorsum of the more painful foot until bending is observed for 3 seconds, followed by a VAS pain rating
Phase 1 - Marijuana subscale (M-scale) of the Addiction Research Center Inventory (ARCI)
The M -scale has 12 true/false statements describing the subjective effects of marijuana
Phase 1 - Neuropsychological Assessment Battery
Testing will include the Wechsler Adult Intelligence Scale (WAIS-III) Digit Symbol, Hopkins Verbal Learning Test-Revised and Grooved Pegboard Test (motor)
Phase 1 - heart rate variability
Heart Rate Variability (HRV) correlates with the level of pain intensity. Persons with effective analgesic treatment of chronic pain exhibited improved HRV relative to pain sufferers with ineffective treatment suggesting HRV may serve as a pain biomarker
Phase 1 - store plasma samples for evaluation of THC, CBD, and endocannabinoid system biomarkers
Cannabinoid and endocannabinoid levels in plasma will be quantified using a liquid chromatography-tandem mass spectrometry (LC/MS)

Full Information

First Posted
March 28, 2017
Last Updated
July 11, 2023
Sponsor
University of California, San Diego
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1. Study Identification

Unique Protocol Identification Number
NCT03099005
Brief Title
Effect of Cannabis and Endocannabinoids on HIV Neuropathic Pain
Official Title
Effect of Cannabis Administration and Endocannabinoids on HIV Neuropathic Pain Primary Study - Phase 2
Study Type
Interventional

2. Study Status

Record Verification Date
July 2023
Overall Recruitment Status
Completed
Study Start Date
July 1, 2018 (Actual)
Primary Completion Date
December 31, 2022 (Actual)
Study Completion Date
December 31, 2022 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
University of California, San Diego

4. Oversight

Studies a U.S. FDA-regulated Drug Product
Yes
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
Yes

5. Study Description

Brief Summary
Acute cannabis administration is reported to alleviate HIV neuropathic pain (HIV-NP), but there is limited knowledge about the effects of cannabis constituents (delta-9 tetrahydrocannabinol/THC and cannabidiol/CBD), the consequences of long-term cannabis use, and the impact of cannabis on endocannabinoid (EC) function in people living with HIV- NP. Our objective is to address these three fundamental gaps in our knowledge by: 1) examining the acute effects of various CBD/THC products on HIV-NP, 2) utilizing a mHealth text messaging protocol, Individual Monitoring of Pain and Cannabis Taken (IMPACT) to monitor daily real-world cannabis use and changes in pain; and 3) studying the relationship between cannabinoids, EC biomarkers, and chronic neuropathic pain
Detailed Description
Our objective is to assess 120 community-dwelling people living with HIV who have neuropathic pain and are currently using cannabis. These participants will be enrolled in a study that consists of two phases: Phase 1) This will involve a cross over study involving three different doses of vaporized cannabis that contain THC and varying concentrations of CBD: Low CBD session: 8 puffs of 1.6% THC + 0.09 CBD Medium CBD sessions: 4 puffs of 1.6% THC + 0.09 CBD plus 4 puffs of 1.73% THC + 5.4% CBD High CBD sessions: 8 puffs of 1.73% THC + 5.4% CBD This phase will examine the acute effects of cannabis on pain intensity, blood endocannabinoid levels, and the relationship of pain with heart rate variability (HRV). Phase 2) This phase will involve the association between dispensary-obtained cannabis and changes in pain reported via IMPACT, a mHealth text messaging program that will serve as a useful tool to monitor the relationship between pain and cannabis use. Text messaging is an effective method to modify health behaviors, monitor substance use, and track pain. Our group has recently demonstrated the feasibility of using short message service (SMS) texting to promote anti-retroviral therapy adherence and monitor daily methamphetamine (METH) use in persons living with HIV neuropathy with bipolar disorder or METH dependence.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Cannabis, HIV Neuropathy, Pain Syndrome
Keywords
neuropathic pain, human immunovirus, vaporized cannabis

7. Study Design

Primary Purpose
Treatment
Study Phase
Phase 2
Interventional Study Model
Crossover Assignment
Model Description
Acutely administered CBD/THC will reduce HIV-neuropathic pain in a stair-step manner; the highest CBD dose will provide the greatest pain reduction (high CBD > medium CBD > low CBD).
Masking
ParticipantCare ProviderInvestigatorOutcomes Assessor
Masking Description
Participants will receive vaporized cannabis using Volcano vaporizers (Storz and Bickel) with either 3.74% THC + 0.49% CBD, 3.49% THC + 4.17% CBD, or 3.11% THC + 15.76% CBD at each of three visits. Allocation assignment of visits will be assigned using a Web-based random number- generating program, "Research Randomizer" (http:// www.randomizer.org/). The allocation schedule will be kept in the pharmacy and concealed from other study personnel.
Allocation
Randomized
Enrollment
44 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Low CBD session
Arm Type
Active Comparator
Arm Description
In the morning, participants will inhale 8 puffs of vaporized cannabis containing 1.6% THC + 0.09 CBD. They will then undergo experimental testing as described below under Outcome Measures.
Arm Title
Medium CBD session
Arm Type
Active Comparator
Arm Description
In the morning, participants will inhale 8 puffs of vaporized cannabis 4 puffs will contain 1.6% THC + 0.09 CBD and 4 puffs will contain 1.73% THC + 5.4% CBD. They will then undergo experimental testing as described below under Outcome Measures.
Arm Title
High CBD session
Arm Type
Active Comparator
Arm Description
In the morning, participants will inhale 8 puffs of vaporized cannabis containing 1.73% THC + 5.4% CBD. They will then undergo experimental testing as described below under Outcome Measures.
Intervention Type
Drug
Intervention Name(s)
Cannabis
Other Intervention Name(s)
marijuana
Intervention Description
vaporization of cannabis
Primary Outcome Measure Information:
Title
Phase 1 - numerical 11-point Pain Intensity Scale
Description
an ordinal scale
Time Frame
participants will be followed for the duration of an 4 hour, single day human laboratory experiment, and the outcome will be measured once before they receive study medication and then 3 additional times during the treatment day
Title
Phase 2 - numerical 11-point Pain Intensity Scale
Description
participants receive interactive text questions sent once a day to their cell phone asking them to indicate their average pain level for the day on a 0 to 10 scale
Time Frame
participants will be queried on a daily basis for six months using text messaging
Secondary Outcome Measure Information:
Title
Phase 1 - Patient Global Impression of Change (PGIC)
Description
a 7 point ordinal scale reflective of improvement in pain
Time Frame
participants will be followed for the duration of an 4 hour, single day human laboratory experiment, and this outcome will be measured 3 times after study medication is provided during the treatment day
Title
Phase 1 - von Frey test
Description
The von Frey filament will be applied on the dorsum of the more painful foot until bending is observed for 3 seconds, followed by a VAS pain rating
Time Frame
participants will be followed for the duration of an 4 hour, single day human laboratory experiment, and the outcome will be measured once before they receive study medication and then 3 additional times during the treatment day
Title
Phase 1 - Marijuana subscale (M-scale) of the Addiction Research Center Inventory (ARCI)
Description
The M -scale has 12 true/false statements describing the subjective effects of marijuana
Time Frame
participants will be followed for the duration of an 4 hour, single day human laboratory experiment, and the outcome will be measured once before they receive study medication and then 3 additional times during the treatment day
Title
Phase 1 - Neuropsychological Assessment Battery
Description
Testing will include the Wechsler Adult Intelligence Scale (WAIS-III) Digit Symbol, Hopkins Verbal Learning Test-Revised and Grooved Pegboard Test (motor)
Time Frame
participants will be followed for the duration of an 4 hour, single day human laboratory experiment, and the outcome will be measured once before they receive study medication and then 3 additional times during the treatment day
Title
Phase 1 - heart rate variability
Description
Heart Rate Variability (HRV) correlates with the level of pain intensity. Persons with effective analgesic treatment of chronic pain exhibited improved HRV relative to pain sufferers with ineffective treatment suggesting HRV may serve as a pain biomarker
Time Frame
participants will be followed for the duration of an 4 hour, single day human laboratory experiment, and the outcome will be measured once before they receive study medication and then 3 additional times during the treatment day
Title
Phase 1 - store plasma samples for evaluation of THC, CBD, and endocannabinoid system biomarkers
Description
Cannabinoid and endocannabinoid levels in plasma will be quantified using a liquid chromatography-tandem mass spectrometry (LC/MS)
Time Frame
participants will be followed for the duration of an 4 hour, single day human laboratory experiment, and the outcome will be measured once before they receive study medication and then 3 additional times during the treatment day

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: the ability to provide informed consent age 18 or older HIV infection documented at the HNRP or assessed by an HIV test at screening; a diagnosis of HIV sensory neuropathy current use of cannabis the ability to describe the THC and CBD content in the products they use, i.e., obtaining cannabis from dispensaries that list THC and CBD content ability to respond to daily text message Exclusion Criteria: meeting criteria for current substance or alcohol dependence traumatic brain injury dementia or Alzheimer's disease psychosis a respiratory condition, i.e., pulmonary disease, that would be exacerbated by inhaling vaporized cannabis history of cardiovascular disease, including myocardial infarction or stroke; uncontrolled hypertension, defined as a systolic blood pressure greater than 160 mm Hg or a diastolic blood pressure greater than 100 mm Hg pregnancy, breastfeeding, or unwillingness to prevent pregnancy during the cannabis administration portion of the study (using birth control in female participants of child- bearing age) unwillingness or inability to receive or respond to text messages
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Brook L Henry, PhD
Organizational Affiliation
University of California, San Diego
Official's Role
Principal Investigator
Facility Information:
Facility Name
UC Center for Medicinal Cannabis Research, UC San Diego
City
San Diego
State/Province
California
ZIP/Postal Code
92103
Country
United States

12. IPD Sharing Statement

Plan to Share IPD
Yes
IPD Sharing Plan Description
The principal investigator, Brook Henry PhD (blhenry@ucsd.edu), will supply individual participant data to other researchers after the project is completed.

Learn more about this trial

Effect of Cannabis and Endocannabinoids on HIV Neuropathic Pain

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