Achieving Cannabis Cessation-Evaluating N-Acetylcysteine Treatment



Status:Completed
Conditions:Psychiatric
Therapuetic Areas:Psychiatry / Psychology
Healthy:No
Age Range:18 - 50
Updated:5/26/2018
Start Date:January 2014
End Date:August 2015

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Achieving Cannabis Cessation: Evaluating N-Acetylcysteine Treatment (ACCENT)

The primary objective of this study is to evaluate the impact of N-acetylcysteine (NAC) 1200
mg versus matched placebo (PBO) twice daily, added to contingency management (CM), on
cannabis use among treatment-seeking cannabis-dependent adults (ages 18-50).

The primary objective of this Phase 3 study is to evaluate the impact of NAC 1200 mg versus
matched placebo (PBO) twice daily, added to contingency management (CM), on cannabis use
among treatment-seeking cannabis-dependent adults (ages 18-50). After assessment and
inclusion into the study, participants will be randomized to receive a 12-week course of NAC
1200 mg or matched placebo twice daily. All participants will concurrently participate in a
twice-weekly contingency management (CM) intervention. Medication management will be
conducted weekly throughout treatment by the medical clinician. Urine cannabinoid testing
will occur at all visits, and will be used as the primary determinant of cannabis use.
Participants will return approximately four weeks after treatment conclusion for evaluation
of adverse events with medication discontinuation and sustained treatment effects.

Inclusion Criteria:

- Age 18-50 years

- Must be able to understand the study and provide written informed consent

- Must meet current DSM-IV criteria for cannabis dependence in the last 30 days

- Must express interest in treatment for cannabis dependence

- Must submit a positive urine cannabinoid test during screening

- Women of child bearing potential must agree to use appropriate birth control methods
during study participation: oral contraceptives, contraceptive patch, barrier
(diaphragm or condom), levonorgestrel implant, medroxyprogesterone acetate, complete
abstinence from sexual intercourse, or hormonal contraceptive vaginal ring

Exclusion Criteria:

- Allergy or intolerance to N-Acetylcysteine

- Women who are pregnant or lactating

- Current use of NAC or any supplement containing N-Acetylcysteine (must agree not to
take any such supplement throughout study participation)

- Use of carbamazepine or nitroglycerin within 14 days of randomization

- Current enrollment in treatment for cannabis dependence

- Any use of synthetic cannabinoids (such as K2/Spice) in the 30 days prior to screening
or during the period between screening and randomization

- Current substance dependence, other than cannabis or nicotine

- Urine drug screen positive for any drug of abuse other than cannabis or amphetamines
at the randomization visit (Only participants who have a valid prescription for
amphetamines (e.g., for ADHD) may be included)

- Urine drug screen positive for amphetamines at the randomization visit without having
a valid prescription for it

- Maintenance treatment with buprenorphine or methadone

- Recent history of asthma (within the last 3 years)

- History of seizure disorder, bipolar disorder, schizophrenia, or other significant or
unstable medical or psychiatric illness that may place the participant at increased
risk in the judgment of the medical clinician

- Significant risk of homicide or suicide
We found this trial at
6
sites
Los Angeles, California 90024
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4502 Medical Drive
San Antonio, Texas 78284
(210) 567-7000
University of Texas Health Science Center at San Antonio The University of Texas Health Science...
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San Antonio, TX
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Lexington, Kentucky
859) 257-9000
University of Kentucky The University of Kentucky is a public, land grant university dedicated to...
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Lexington, KY
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New Haven, Connecticut 06519
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New Haven, CT
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Pickens, South Carolina 29671
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Pickens, SC
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Portland, Oregon 97214
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Portland, OR
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