ConductScience.org, home

Trial · NCT01675661

Achieving Cannabis Cessation-Evaluating N-Acetylcysteine Treatment

NCT01675661, Phase 3, Completed, Medical University of South Carolina; results first posted 2017-03-08

3 sourcestrials-2026-11-12-0.5.0

Download JSON
Cite this record

ConductScience Library. Achieving Cannabis Cessation-Evaluating N-Acetylcysteine Treatment. Trials, record NCT01675661. Release trials-2026-11-12-0.5.0, 12 Nov 2026. https://conductscience.org/library/trials/NCT01675661

On this page

Trial

As registered on ClinicalTrials.gov, in the graph's capture of the registry.

Title
Achieving Cannabis Cessation-Evaluating N-Acetylcysteine Treatment
NCT number
NCT01675661
Status
Completed
Phases
Phase 3
Enrollment
302 participants, actual
Lead sponsor
Medical University of South Carolina
Conditions
Cannabis Dependence
Interventions
N-Acetylcysteine, Placebo
First posted
2012-08-30
Last updated
2018-05-24
Results first posted
2017-03-08

Source ClinicalTrials.gov

Registered outcomes1

Each outcome the trial registered, primary first, in ClinicalTrials.gov's words.

ListOutcomeTime frameDescription
PrimaryThe Odds of Negative Urine Cannabinoid Tests During Treatment.study weeks 2-13
The primary outcome is the abstinence rate over the 12 weeks of treatment. Abstinence is based on a weekly urine drug screen confirmed by central laboratory testing and defined as a negative cannabinoid result.

Outcomes1

Each outcome the trial posted results for, in ClinicalTrials.gov's words.

TypeOutcomeTime framePopulationUnitsMeasured as
PRIMARYThe Odds of Negative Urine Cannabinoid Tests During Treatment.study weeks 2-13Intent to treat; all participants randomizedcannabis negative urine testsNUMBER

Results by group26

Each measurement the trial posted, group by group, in the words and numbers it posted.

OutcomeGroupCategoryValueSpreadUnits
The Odds of Negative Urine Cannabinoid Tests During Treatment.NAC Plus CMStudy Week 225cannabis negative urine tests
The Odds of Negative Urine Cannabinoid Tests During Treatment.Placebo Plus CMStudy Week 221cannabis negative urine tests
The Odds of Negative Urine Cannabinoid Tests During Treatment.NAC Plus CMStudy Week 330cannabis negative urine tests
The Odds of Negative Urine Cannabinoid Tests During Treatment.Placebo Plus CMStudy Week 322cannabis negative urine tests
The Odds of Negative Urine Cannabinoid Tests During Treatment.NAC Plus CMStudy Week 433cannabis negative urine tests
The Odds of Negative Urine Cannabinoid Tests During Treatment.Placebo Plus CMStudy Week 436cannabis negative urine tests
The Odds of Negative Urine Cannabinoid Tests During Treatment.NAC Plus CMStudy Week 532cannabis negative urine tests
The Odds of Negative Urine Cannabinoid Tests During Treatment.Placebo Plus CMStudy Week 533cannabis negative urine tests
The Odds of Negative Urine Cannabinoid Tests During Treatment.NAC Plus CMStudy Week 632cannabis negative urine tests
The Odds of Negative Urine Cannabinoid Tests During Treatment.Placebo Plus CMStudy Week 630cannabis negative urine tests

Participant flow6

How many started, completed or left each group, period by period.

PeriodMilestoneGroupParticipantsUnits counted
Overall StudySTARTEDNAC Plus CM153
Overall StudySTARTEDPlacebo Plus CM149
Overall StudyCOMPLETEDNAC Plus CM113
Overall StudyCOMPLETEDPlacebo Plus CM103
Overall StudyNOT COMPLETEDNAC Plus CM40
Overall StudyNOT COMPLETEDPlacebo Plus CM46

Adverse events106

Each adverse event the trial posted, group by group: the participants affected out of those at risk.

TypeEventOrgan systemGroupAffectedAt riskEvents
otherNauseaGastrointestinal disordersNAC Plus CM71537
otherNauseaGastrointestinal disordersPlacebo Plus CM1014910
otherDiarrheaGastrointestinal disordersNAC Plus CM81538
otherDiarrheaGastrointestinal disordersPlacebo Plus CM81498
otherAbdominal discomfortGastrointestinal disordersNAC Plus CM31533
otherAbdominal discomfortGastrointestinal disordersPlacebo Plus CM51495
otherDyspepsiaGastrointestinal disordersNAC Plus CM31533
otherDyspepsiaGastrointestinal disordersPlacebo Plus CM11491
otherFlatulenceGastrointestinal disordersNAC Plus CM01530
otherFlatulenceGastrointestinal disordersPlacebo Plus CM21492

Adverse event totals6

The totals the trial posted for each group.

TotalGroupAffectedAt risk
Total, all-cause mortalityNAC Plus CM
Total, all-cause mortalityPlacebo Plus CM
Total, other adverse eventsNAC Plus CM40153
Total, other adverse eventsPlacebo Plus CM45149
Total, serious adverse eventsNAC Plus CM1153
Total, serious adverse eventsPlacebo Plus CM6149

Papers6

The papers the trial lists on ClinicalTrials.gov.

PMIDListed asSource
25179587BACKGROUNDPubMed
28623823DERIVEDPubMed
28847455DERIVEDPubMed
31712969DERIVEDPubMed
34197135DERIVEDPubMed
35084903DERIVEDPubMed

Grants7

The grants NIH RePORTER links to the trial, newest funded first: NIH's, and some of AHRQ's, CDC's, FDA's and VA's. Each shows its title, principal investigators, organization and funder in its newest year.

ProjectTitlePrincipal investigatorsOrganizationFunderFiscal yearsSource
UG1DA013727Southern Consortium Node of the Clinical Trials NetworkBARTH, KELLY S.; BRADY, KATHLEEN T.MEDICAL UNIVERSITY OF SOUTH CAROLINANATIONAL INSTITUTE ON DRUG ABUSE2015 to 2025NIH RePORTER
U10DA013045The National Drug Abuse Treatment Clinical Trials NetworkLING, WALTER NMNUNIVERSITY OF CALIFORNIA LOS ANGELESNATIONAL INSTITUTE ON DRUG ABUSE1999 to 2015NIH RePORTER
U10DA013727Southern Consortium Node of the Clinical Trials NetworkBRADY, KATHLEEN T.MEDICAL UNIVERSITY OF SOUTH CAROLINANATIONAL INSTITUTE ON DRUG ABUSE2000 to 2015NIH RePORTER
U10DA013732Clinical Trials Network, Ohio Valley Node U10DA013732WINHUSEN, T JOHNUNIVERSITY OF CINCINNATINATIONAL INSTITUTE ON DRUG ABUSE2000 to 2015NIH RePORTER
U10DA015815Western States Node of the National Drug Abuse Treatment Clinical Trials NetworkSORENSEN, JAMES L; MCCARTY, DENNISUNIVERSITY OF CALIFORNIA, SAN FRANCISCONATIONAL INSTITUTE ON DRUG ABUSE2002 to 2015NIH RePORTER
U10DA015831The National Drug Abuse Treatment Clinical Trials Network (U10)WEISS, ROGER D.; CARROLL, KATHLEEN M.MCLEAN HOSPITALNATIONAL INSTITUTE ON DRUG ABUSE2002 to 2015NIH RePORTER
U10DA020024Clinical Trials Network: The Texas NodeTRIVEDI, MADHUKAR H.UT SOUTHWESTERN MEDICAL CENTERNATIONAL INSTITUTE ON DRUG ABUSE2005 to 2015NIH RePORTER

Trial comparisons1

Comparisons of the trial's two groups, calculated by ConductScience from the counts it posted.

Comparison
NAC Plus CM vs Placebo Plus CM: serious adverse events

Tests0

The ConductCognition tests this trial's registered outcomes name, as ScienceGraph matched them in trial-tests-2026-11-12-0.2.1.

None in this release.

Data dates

The day each source was copied for this release.

ClinicalTrials.gov
2026-11-12
ClinicalTrials.gov
Results, from AACT
2026-03-23
AACT
NIH grant links
2026-11-13
NIH RePORTER

Sources 3

  • ClinicalTrials.gov's posted results, through CTTI's AACTFreely available. Acknowledgement requested
  • ClinicalTrials.govNo license stated
  • NIH RePORTER's clinical studies and project filesPublic domain
Each source's terms
  • ClinicalTrials.gov's posted results, through CTTI's AACTClinicalTrials.gov data via Aggregate Analysis of ClinicalTrials.gov (AACT), CTTI. CTTI makes its materials freely available and requests acknowledgement. https://aact.ctti-clinicaltrials.org/documentation/299
  • ClinicalTrials.govnone stated
  • NIH RePORTER's clinical studies and project filesPublic domain (NIH RePORTER)

ClinicalTrials.gov's data carry an international copyright outside the United States: https://clinicaltrials.gov/about-site/terms-conditions.

For software

Read this trial from software.

The record and each of its lists are JSON, twenty rows a page. No key.

GET https://conductscience.org/api/trials/v1/NCT01675661

GET https://conductscience.org/api/trials/v1/NCT01675661/results?page=2