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SV2A Density Cannabis Use Disorder

SV2A Density Cannabis Use Disorder

Status
Recruiting
Phases
Early Phase 1
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT05472818
Enrollment
51
Registered
2022-07-25
Start date
2022-04-12
Completion date
2032-05-01
Last updated
2026-03-12

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Cannabis Use Disorder, Healthy

Keywords

Cannabis Use Disorder (CUD), Healthy subjects, synaptic vesicle density, [11C]APP311, UCB-J

Brief summary

The main purpose of this study is to determine whether hippocampal synaptic vesicle density estimated by hippocampal \[11C\]APP-311/\[11C\]UCB-J binding in individuals diagnosed with cannabis use disorder (CUDs) improves with at least 4 weeks of confirmed abstinence from cannabis, in comparison to healthy controls (HCs). Furthermore, any change in synaptic vesicle density will be placed in functional context by measuring verbal memory, which is sensitive to hippocampal function, before and after at least 4 weeks of confirmed abstinence. Finally, the relationship between hippocampal \[11C\]UCB-J binding in CUDs with measures of cannabis exposure (e.g., age of initiation, cumulative lifetime dose) will be explored.

Interventions

For each \[11C\]APP311 (UCB-J) PET scan, up to 20 mCi of \[11C\]APP311 (UCB-J) will be administered by infusion pump. All participants will receive at least two \[11C\]APP311 (UCB-J) PET scans approx. 4 weeks days apart. Approximately 8 CUD participants will be asked to return for a third \[11C\]APP311 (UCB-J) PET scan after an additional 4 weeks following their second scan.

Sponsors

Yale University
Lead SponsorOTHER
National Institute on Drug Abuse (NIDA)
CollaboratorNIH

Study design

Allocation
NON_RANDOMIZED
Intervention model
PARALLEL
Primary purpose
BASIC_SCIENCE
Masking
NONE

Intervention model description

In this study, patients with cannabis use disorder (CUD) and matched healthy controls will be scanned using anatomical magnetic resonance imaging (MRI) and PET. All participants will receive two PET scans, 4 weeks apart. CUD participants will be asked to abstain from cannabis for the 4 week period. A small subset of CUD participants will be asked to continue abstaining for an additional approx. 4 weeks to complete one additional scan. Participants may also complete a neurocognitive battery, various psychiatric evaluations, a physical examination, an ECG, blood tests, and questionnaires. CUD participants will complete bi-weekly study visits to confirm abstinence.

Eligibility

Sex/Gender
ALL
Age
18 Years to 75 Years
Healthy volunteers
Yes

Inclusion criteria

CUD Participants Inclusion Criteria: 1. Able to provide informed consent 2. Male and female 18-75 years old 3. Daily cannabis use 4. Positive urine screen for cannabinoids and negative for all other drugs on 5. Diagnosis of DSM-5 cannabis use disorder (≥ moderate, i.e., ≥ 4 \[of 11\] symptoms). 6. Must express a willingness at screening to set a date to attempt to quit using cannabis. 7. Physically healthy i.e., no clinically unstable medical conditions. 8. For women of childbearing potential (WOCBP) and men, willingness to practice birth control and to inform study staff immediately if either they (for women) or their partner (for men) becomes pregnant. 9. Additional criteria not disclosed here in order to minimize the risk of ineligible subjects enrolling in the study. CUD Participants

Exclusion criteria

1. Laboratory tests with clinically significant abnormalities or positive urine toxicology screen with exception of cannabinoids. 2. Women with a positive pregnancy test or women who are lactating. 3. Have implanted or embedded metal objects or fragments in the head or body that would present a risk during the MRI scanning procedure, or have worked with ferrous metals either as a vocation or hobby (for example, as a sheet metal worker, welder, or machinist) in such a way that might have led to unknown, indwelling metal fragments that could cause injury if they moved in response to placement in the magnetic field 4. Have had exposure to ionizing radiation that in combination with the study tracer would result in a cumulative exposure that exceeds recommended exposure limits. 5. History of a bleeding disorder or are currently taking anticoagulants (such as Coumadin, Heparin, Pradaxa, Xarelto) Subjects who have donated blood within 8 weeks of the present study 6. Medications that could alter synaptic density and, therefore, confound the interpretation of study data. 7. Additional criteria not disclosed here in order to minimize the risk of ineligible subjects enrolling in the study. Healthy Controls Inclusion Criteria: 1. Willing and able to give voluntary written informed consent 2. Male and Female subjects, age 18 to 75 years, inclusive 3. BMI within 19 to 35 kg/m2, inclusive 4. Must be in good health as determined by medical history, physical examination, ECG, serum/urine biochemistry, hematology, and serology tests. 5. Negative urine drug screen 6. If female, not pregnant or breastfeeding 7. If female of childbearing potential, must agree to use an acceptable method of birth control, as determined by the principal investigator, for the duration of the study and up to one month after completion of PET scans. 8. Able to read and write, able to communicate effectively with the investigator, and comply with all study requirements, restrictions, and directions of the clinic staff. 9. Have arterial access sufficient to allow blood sampling as per the protocol. Healthy Controls

Design outcomes

Primary

MeasureTime frameDescription
Hippocampal SV2A synaptic densityAll participants will receive at least two [11C]APP311 (UCB-J) PET scans approx. 4 weeks days apart.Hippocampal SV2A synaptic density will be measured using \[11C\]APP311 (UCB-J).

Secondary

MeasureTime frameDescription
Hippocampal binding and Hippocampal Verbal Memory TaskThe Auditory Verbal Learning Task (AVLT) will be administered before and after the 4 week abstinence period.To determine the relationship between hippocampal \[11C\]APP311 (UCB-J) binding and performance on the hippocampal verbal memory task (Auditory Verbal Learning Task \[AVLT\]), a cognitive task that measures total immediate recall, before and after 4 weeks of confirmed cannabis abstinence.
Hippocampal binding and Groton Maze Learning in CUDsThe Groton Maze Learning Task will be administered before and after the 4 week abstinence period.To determine the relationship between hippocampal \[11C\]APP311 (UCB-J) binding and performance on the Groton Maze Learning task, a cognitive task that measures total number of errors, in CUDs before and after 4 weeks of confirmed cannabis abstinence.

Countries

United States

Contacts

CONTACTShannon Zeilman
shannon.zeilman@yale.edu203-974-7822
PRINCIPAL_INVESTIGATORDeepak C D'Souza

Yale University

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Mar 13, 2026