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
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.
| List | Outcome | Time frame | Description |
|---|---|---|---|
| Primary | The 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. |
Source ClinicalTrials.gov
Outcomes1
Each outcome the trial posted results for, in ClinicalTrials.gov's words.
| Type | Outcome | Time frame | Population | Units | Measured as |
|---|---|---|---|---|---|
| PRIMARY | The Odds of Negative Urine Cannabinoid Tests During Treatment. | study weeks 2-13 | Intent to treat; all participants randomized | cannabis negative urine tests | NUMBER |
Source ClinicalTrials.gov
Results by group26
Each measurement the trial posted, group by group, in the words and numbers it posted.
| Outcome | Group | Category | Value | Spread | Units |
|---|---|---|---|---|---|
| The Odds of Negative Urine Cannabinoid Tests During Treatment. | NAC Plus CM | Study Week 2 | 25 | cannabis negative urine tests | |
| The Odds of Negative Urine Cannabinoid Tests During Treatment. | Placebo Plus CM | Study Week 2 | 21 | cannabis negative urine tests | |
| The Odds of Negative Urine Cannabinoid Tests During Treatment. | NAC Plus CM | Study Week 3 | 30 | cannabis negative urine tests | |
| The Odds of Negative Urine Cannabinoid Tests During Treatment. | Placebo Plus CM | Study Week 3 | 22 | cannabis negative urine tests | |
| The Odds of Negative Urine Cannabinoid Tests During Treatment. | NAC Plus CM | Study Week 4 | 33 | cannabis negative urine tests | |
| The Odds of Negative Urine Cannabinoid Tests During Treatment. | Placebo Plus CM | Study Week 4 | 36 | cannabis negative urine tests | |
| The Odds of Negative Urine Cannabinoid Tests During Treatment. | NAC Plus CM | Study Week 5 | 32 | cannabis negative urine tests | |
| The Odds of Negative Urine Cannabinoid Tests During Treatment. | Placebo Plus CM | Study Week 5 | 33 | cannabis negative urine tests | |
| The Odds of Negative Urine Cannabinoid Tests During Treatment. | NAC Plus CM | Study Week 6 | 32 | cannabis negative urine tests | |
| The Odds of Negative Urine Cannabinoid Tests During Treatment. | Placebo Plus CM | Study Week 6 | 30 | cannabis negative urine tests |
1 to 10 of 26Source ClinicalTrials.gov
See all 26 results by groupParticipant flow6
How many started, completed or left each group, period by period.
| Period | Milestone | Group | Participants | Units counted |
|---|---|---|---|---|
| Overall Study | STARTED | NAC Plus CM | 153 | |
| Overall Study | STARTED | Placebo Plus CM | 149 | |
| Overall Study | COMPLETED | NAC Plus CM | 113 | |
| Overall Study | COMPLETED | Placebo Plus CM | 103 | |
| Overall Study | NOT COMPLETED | NAC Plus CM | 40 | |
| Overall Study | NOT COMPLETED | Placebo Plus CM | 46 |
Source ClinicalTrials.gov
Adverse events106
Each adverse event the trial posted, group by group: the participants affected out of those at risk.
| Type | Event | Organ system | Group | Affected | At risk | Events |
|---|---|---|---|---|---|---|
| other | Nausea | Gastrointestinal disorders | NAC Plus CM | 7 | 153 | 7 |
| other | Nausea | Gastrointestinal disorders | Placebo Plus CM | 10 | 149 | 10 |
| other | Diarrhea | Gastrointestinal disorders | NAC Plus CM | 8 | 153 | 8 |
| other | Diarrhea | Gastrointestinal disorders | Placebo Plus CM | 8 | 149 | 8 |
| other | Abdominal discomfort | Gastrointestinal disorders | NAC Plus CM | 3 | 153 | 3 |
| other | Abdominal discomfort | Gastrointestinal disorders | Placebo Plus CM | 5 | 149 | 5 |
| other | Dyspepsia | Gastrointestinal disorders | NAC Plus CM | 3 | 153 | 3 |
| other | Dyspepsia | Gastrointestinal disorders | Placebo Plus CM | 1 | 149 | 1 |
| other | Flatulence | Gastrointestinal disorders | NAC Plus CM | 0 | 153 | 0 |
| other | Flatulence | Gastrointestinal disorders | Placebo Plus CM | 2 | 149 | 2 |
1 to 10 of 106Source ClinicalTrials.gov
See all 106 adverse eventsAdverse event totals6
The totals the trial posted for each group.
| Total | Group | Affected | At risk |
|---|---|---|---|
| Total, all-cause mortality | NAC Plus CM | ||
| Total, all-cause mortality | Placebo Plus CM | ||
| Total, other adverse events | NAC Plus CM | 40 | 153 |
| Total, other adverse events | Placebo Plus CM | 45 | 149 |
| Total, serious adverse events | NAC Plus CM | 1 | 153 |
| Total, serious adverse events | Placebo Plus CM | 6 | 149 |
Source ClinicalTrials.gov
Papers6
The papers the trial lists on ClinicalTrials.gov.
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.
| Project | Title | Principal investigators | Organization | Funder | Fiscal years | Source |
|---|---|---|---|---|---|---|
| UG1DA013727 | Southern Consortium Node of the Clinical Trials Network | BARTH, KELLY S.; BRADY, KATHLEEN T. | MEDICAL UNIVERSITY OF SOUTH CAROLINA | NATIONAL INSTITUTE ON DRUG ABUSE | 2015 to 2025 | NIH RePORTER |
| U10DA013045 | The National Drug Abuse Treatment Clinical Trials Network | LING, WALTER NMN | UNIVERSITY OF CALIFORNIA LOS ANGELES | NATIONAL INSTITUTE ON DRUG ABUSE | 1999 to 2015 | NIH RePORTER |
| U10DA013727 | Southern Consortium Node of the Clinical Trials Network | BRADY, KATHLEEN T. | MEDICAL UNIVERSITY OF SOUTH CAROLINA | NATIONAL INSTITUTE ON DRUG ABUSE | 2000 to 2015 | NIH RePORTER |
| U10DA013732 | Clinical Trials Network, Ohio Valley Node U10DA013732 | WINHUSEN, T JOHN | UNIVERSITY OF CINCINNATI | NATIONAL INSTITUTE ON DRUG ABUSE | 2000 to 2015 | NIH RePORTER |
| U10DA015815 | Western States Node of the National Drug Abuse Treatment Clinical Trials Network | SORENSEN, JAMES L; MCCARTY, DENNIS | UNIVERSITY OF CALIFORNIA, SAN FRANCISCO | NATIONAL INSTITUTE ON DRUG ABUSE | 2002 to 2015 | NIH RePORTER |
| U10DA015831 | The National Drug Abuse Treatment Clinical Trials Network (U10) | WEISS, ROGER D.; CARROLL, KATHLEEN M. | MCLEAN HOSPITAL | NATIONAL INSTITUTE ON DRUG ABUSE | 2002 to 2015 | NIH RePORTER |
| U10DA020024 | Clinical Trials Network: The Texas Node | TRIVEDI, MADHUKAR H. | UT SOUTHWESTERN MEDICAL CENTER | NATIONAL INSTITUTE ON DRUG ABUSE | 2005 to 2015 | NIH 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 |
Source Trial comparisons
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.
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