Vitamin D and Cocaine Administration

Sponsor
Yale University (Other)
Overall Status
Suspended
CT.gov ID
NCT04826133
Collaborator
(none)
24
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2
59.2
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Study Details

Study Description

Brief Summary

This study is designed to explore the effects of acute pre-treatment with 1,25-dihydroxyvitamin D3 (calcitriol), as compared to placebo on the behavioral (e.g., attempts to self-administer and ultimate number of infusions/boluses of cocaine self-administered), neurocognitive (e.g., performance on computerized tests of reward related learning such as the probabilistic selection task or PST and probabilistic reward task or PRT), and subjective effects (e.g, computerized visual analog scale [VAS] ratings of euphoria/, craving, etc.) of cocaine in experienced, non-treatment seeking users of the drug.

Condition or Disease Intervention/Treatment Phase
Early Phase 1

Study Design

Study Type:
Interventional
Anticipated Enrollment :
24 participants
Allocation:
Randomized
Intervention Model:
Single Group Assignment
Masking:
Double (Participant, Investigator)
Primary Purpose:
Treatment
Official Title:
Testing Restoring Effects of Vitamin D on the Dopamine System: A Human Laboratory Study Among Cocaine Users.
Actual Study Start Date :
Mar 27, 2019
Anticipated Primary Completion Date :
Mar 1, 2024
Anticipated Study Completion Date :
Mar 1, 2024

Arms and Interventions

Arm Intervention/Treatment
Active Comparator: Acute Pretreatment with Calcitriol

To explore the effects of acute pre-treatment with Calcitriol on attempts to self-administer and ultimate number of infusions/boluses of cocaine, in experienced, non treatment-seeking users of the drug

Drug: Calcitriol
Subjects will receive an oral administration of calcitriol (1,25-dihydroxyvitamin D3) 1.5 μg (three capsules of 0.5 μg each) at 9 pm, night before each cocaine session, and at 8 am, morning of each cocaine session. This dose of calcitriol is lower than doses safely administered in other human studies and for a duration of time shorter than doses safely administered in other trials. In addition, this dose has been already tested by our group, subject of a different grant application, and should be effective at enhancing stimulant's induced dopamine release, in comparison to placebo.
Other Names:
  • 1,25-dihydroxyvitamin D3
  • Placebo Comparator: Acute Pretreatment with Placebo

    To explore the effects of acute pre-treatment with placebo on attempts to self-administer and ultimate number of infusions/boluses of cocaine, in experienced, non treatment-seeking users of the drug

    Other: Placebo
    Subjects will receive an oral administration of three capsules of placebo at 9 pm the night before each cocaine session, and at 8 am, morning of each cocaine session.

    Outcome Measures

    Primary Outcome Measures

    1. Cocaine Self Administration Attempts [90 minutes]

      Number of attempts to self administer cocaine will be analyzed.

    2. Cocaine Self Administration Infusions [90 minutes]

      Number of infusions of cocaine will be analyzed.

    Secondary Outcome Measures

    1. Probabilistic Selection Task (PST) [15 minutes]

      The Probabilistic Selection Task (PST) is a computerized task that assesses the tendency to learn from positive versus negative outcomes. PST will be analyzed using linear mixed models with treatment and time included as a within subjects variable.

    2. Probabilistic Reward Task (PRT) [15 minutes]

      The Probabilistic Reward Task (PRT) is a computerized task that uses an asymmetric reinforcement schedule to produce a response bias towards the more frequently rewarded of two possible stimuli. PRT will be analyzed using linear mixed models with treatment and time included as a within subjects variable.

    3. Subjective Effects of Cocaine / Visual Analog Scale (VAS) [150 minutes]

      During cocaine sessions, subjects will complete a series of self rated subjective effects measuring how they feel on cocaine, using a scale of 0 (not at all) to 10 (most ever). VAS ratings will focus on euphoria ("high") as a primary outcome, however, other positive, negative, psychomotor, and drug-craving ratings (e.g. good, bad, stimulated, paranoid, hungry, etc.) will be collected as well. Ratings are implemented on a touch-screen laptop computer and presented every 5 minutes, throughout the session

    Eligibility Criteria

    Criteria

    Ages Eligible for Study:
    30 Years to 55 Years
    Sexes Eligible for Study:
    All
    Accepts Healthy Volunteers:
    No
    Inclusion Criteria:
    • Age 30-55 years

    • Voluntary, written, informed consent

    • Physically healthy by medical history, physical, neurological, ECG and laboratory examinations

    • DSM-5 criteria for at least moderate Cocaine Use Disorder

    • Recent street cocaine use in excess of quantities used in the current study

    • Intravenous and/or smoked (crack/ freebase) use

    • Positive urine toxicology screen for cocaine

    • Laboratory evidence of vitamin D sufficiency (i.e., 25(OH)-vitamin D3 level ≥ 20/mg)

    • For females, a negative serum pregnancy (HCG) test at screening and admission, and a negative urine pregnancy test (HCG) on cocaine administration days.

    Exclusion Criteria:
    • A history of other substance dependence (except for nicotine). Positive urine toxicology for cannabis is accepted for the study unless there is evidence for dependence per Structured Clinical Interview for DSM-5 (SCID) interview. Positive urine toxicology for other drugs at screening will be repeated. If positive again and/or positive at admission, subjects will be excluded

    • < 1 year of cocaine abuse/dependence

    • A primary DSM-5 Axis I major psychiatric disorder (e.g., schizophrenia, bipolar disorder, major depression, etc.) unrelated to cocaine as determined by the SCID-5

    • Medical comorbidities including serum calcium ( > 10.5 mg/dl, serum phosphorus > 4.2 mg/dl), hyperparathyroidism, kidney disease (e.g., Serum creatinine > 1.3 mg/dl)

    • A history of significant and uncontrolled medical (e.g., cardiovascular, diabetic/metabolic) or neurological (e.g., cerebrovascular, seizures, traumatic brain injury) illness

    • A history of seizures

    • Current use of psychotropic/potentially psychoactive medications or medications that can have drug drug interactions with calcitriol, including over the counter Vitamin D products, thiazide diuretics, and calcium supplements, etc, as referenced in the package insert for calcitriol

    • Seeking treatment for drug abuse/dependence

    • Hypersensitivity to calcitriol

    • For females, physical or laboratory (HCG) evidence of pregnancy.

    Contacts and Locations

    Locations

    Site City State Country Postal Code
    1 Connecticut Mental Health Center New Haven Connecticut United States 06519

    Sponsors and Collaborators

    • Yale University

    Investigators

    • Principal Investigator: Marc Potenza, MD, PhD, Yale University

    Study Documents (Full-Text)

    None provided.

    More Information

    Publications

    None provided.
    Responsible Party:
    Marc Potenza, Principal Investigator, Yale University
    ClinicalTrials.gov Identifier:
    NCT04826133
    Other Study ID Numbers:
    • 2000025367
    First Posted:
    Apr 1, 2021
    Last Update Posted:
    Jul 13, 2022
    Last Verified:
    Jul 1, 2022
    Studies a U.S. FDA-regulated Drug Product:
    Yes
    Studies a U.S. FDA-regulated Device Product:
    No
    Additional relevant MeSH terms:

    Study Results

    No Results Posted as of Jul 13, 2022