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NAC for Treating Comorbid PTSD and SUD

Glial Regulators for Treating Comorbid Posttraumatic Stress Disorder and Substance Use Disorders

Status
Completed
Phases
Phase 2
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT02911285
Acronym
DoD-NAC
Enrollment
90
Registered
2016-09-22
Start date
2016-10-31
Completion date
2019-11-04
Last updated
2021-05-19

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

Conditions

Alcohol Use Disorder (AUD), Posttraumatic Stress Disorder (PTSD), Substance Use Disorder (SUD)

Keywords

Alcohol, PTSD, Trauma, Veteran, Substance, Drug, Post Traumatic Stress Disorder, Military

Brief summary

As a result of sustained operations in Afghanistan and Iraq, there are an increasing number of U.S. military Veterans with substance use disorders and comorbid posttraumatic stress disorder (PTSD). If left untreated, individuals with substance use disorders and PTSD are at increased risk for developing other mental health problems (e.g., depression, anxiety), suicidal ideation and attempts, medical problems, reduced resiliency and military readiness, vocational problems, and family/social impairment. This study will determine the benefits of N-acetylcysteine (NAC) in treating alcohol use disorder and comorbid post-traumatic stress disorder (PTSD) among military Veterans.

Detailed description

As a result of sustained operations in Afghanistan and Iraq, there are an increasing number of U.S. military Veterans with substance use disorders and comorbid posttraumatic stress disorder (PTSD). While mental health services are in place for U.S. service members, substantial gaps in the treatment of co-occurring substance use disorders and PTSD exist and there is little scientific evidence available to guide the provision of care. Treatment for comorbid substance use disorders and PTSD, especially pharmacologic treatment, is largely ineffective and short-lived. While there have been numerous studies focused largely on dopaminergic mechanisms of reward, they have not led to the development of adequate treatments for comorbid substance use disorders and PTSD. Animal models demonstrate that (a) acute stress and chronic use of addictive substances reduce the capacity of glia to remove the neurotransmitter glutamate, and (b) this impairment as well as relapse can be prevented or reversed by N-acetylcysteine (NAC). Further, human studies indicate that NAC is associated with reduced craving and substance use. Based on this, the investigators conducted a Proof of Principle (PoP) study which was the first to examine the use of NAC for the treatment of PTSD, with or without comorbid addiction. In this randomized, controlled double-blind pilot study the investigators showed that Veterans with substance use disorders (81.5% alcohol use disorder) and PTSD who were treated with 2400mg NAC for 8 weeks demonstrated significant reduction in PTSD severity and craving. Moreover, reductions in PTSD and substance-related symptomatology were sustained at 1-month follow-up. However, to extend and confirm its clinical utility in the military/Veteran context, it is important to know whether NAC reduces severity of alcohol use disorder (AUD), the most common addiction among Veterans and military service members, and the mechanisms underlying therapeutic response. Based on promising data from the PoP project, the proposed Extend-and-Confirm (EC) study will determine the efficacy of NAC in reducing AUD and comorbid PTSD in Veterans (N=90). Further, new aims include the application of functional magnetic resonance imaging (fMRI) and proton magnetic resonance spectroscopy (1H-MRS) to investigate the pathophysiology of AUD/PTSD, as well as prognostic indicators of treatment outcome. These aims extend the Future Plans proposed in the original PoP study and provide an opportunity for collaboration among clinical and preclinical investigators at the Ralph H. Johnson Veterans Affairs (VA) Medical Center and the Medical University of South Carolina (MUSC) to solve this critical health problem in the military context. In the proposed EC study, the investigators will (1) employ a randomized, double-blind, between-groups experimental design that will consist of 8 weeks of treatment with NAC (2400mg) or placebo medication, and follow-up assessment at 1-, 3-, and 6-months post treatment; (2) use standardized, repeated dependent measures to rigorously assess AUD severity and PTSD symptomatology during treatment and follow-up; (3) collect biologic measures of alcohol use; (4) measure impairment in associated areas of functioning (e.g., depression, sleep, suicidality, risky sexual behaviors, family/social functioning); and (5) employ advanced neuroimaging techniques before and after treatment among a subset of enrolled subjects. This proposal is directly responsive to the missions of the Institute for Translational Neuroscience (ITN), and the US Army/Department of Defense (DoD) in that it seeks to accelerate the development of new, medication-based treatments to mitigate the impact of AUD and comorbid psychological conditions, such as PTSD, in the military/Veteran context. The findings of this study will provide critically needed empirical evidence to help inform practice guidelines and better serve the needs of U.S. service members, Veterans and their families.

Interventions

DRUGN-acetylcysteine

1200mg bid (2400mg/day)

DRUGPlacebo

Placebo pills bid

BEHAVIORALCognitive behavioral therapy

CBT for AUD/SUD, one hour/once a week

Sponsors

United States Department of Defense
CollaboratorFED
Institute for Translational Neuroscience
CollaboratorUNKNOWN
Medical University of South Carolina
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
TRIPLE (Subject, Caregiver, Investigator)

Eligibility

Sex/Gender
ALL
Age
18 Years to 75 Years
Healthy volunteers
No

Inclusion criteria

* Male or female, any race or ethnicity, age 18 to 75 years old. * U.S. military Veteran, including National Guard and Reservists. * Able to comprehend English. * Meet Diagnostic and Statistical Manual (DSM-5) criteria for current alcohol use disorder (AUD) and/or substance use disorder (SUD). * Meet DSM-5 criteria for current PTSD or subthreshold PTSD. Subjects may also meet criteria for a mood disorder (except bipolar affective disorder, see

Exclusion criteria

) or other anxiety disorders (e.g., panic disorder, agoraphobia, social phobia, generalized anxiety disorder). The inclusion of subjects with affective and other anxiety disorders is essential because of the marked frequency of the co-existence of mood and other anxiety disorders among patients with PTSD (Brady et al., 2000; Kessler et al., 2005). * Subjects taking psychotropic medications will be required to be maintained on a stable dose for at least four weeks before treatment initiation. This is because initiation or change of medications during the course of the trial may interfere with interpretation of results. * Must consent to random assignment to N-acetylcysteine (NAC) or placebo. * Must consent to complete all treatment and follow-up visits.

Design outcomes

Primary

MeasureTime frameDescription
Change in Alcohol Use Disorder SeverityFrom baseline to week 8 of treatmentChange in Alcohol Use Disorder Severity as measured by change in average drinking days per week from baseline to week 8. Greater reduction in drinking days indicates better treatment outcomes. Drinking days measured over 1 week periods (7 days). Scale ranges from 0 days to 7 days.
Change in Post Traumatic Stress Disorder SeverityFrom baseline to week 8Change in post traumatic stress disorder severity as measured by Change in Clinician Administered PTSD Scale (CAPS-5) score from baseline to week 8. Greater change/reduction in score indicates better outcomes and greater reduction in PTSD symptomatology. (minimum score of 0 = absent to a maximum score of 80 = extreme)
Change in Alcohol CravingFrom baseline to week 8Change in Alcohol craving as measured by change in Obsessive Compulsive Drinking Scale (OCDS) Total Score. Greater change/reduction in score indicates better outcomes and reduced alcohol craving. (Scores range from 0 to 56)

Countries

United States

Participant flow

Participants by arm

ArmCount
N-acetylcysteine + Cognitive Behavioral Therapy
Participants received N-acetylcysteine (NAC) and Cognitive Behavioral Therapy (CBT) for 8 weeks. N-acetylcysteine: 1200mg bid (2400mg/day) Cognitive behavioral therapy: CBT for AUD/SUD, one hour/once a week
49
Placebo + Cognitive Behavioral Therapy
Participants received placebo pills and CBT for 8 weeks. Placebo: Placebo pills bid Cognitive behavioral therapy: CBT for AUD/SUD, one hour/once a week
41
Total90

Withdrawals & dropouts

PeriodReasonFG000FG001
Overall StudyLost to Follow-up85
Overall StudyParticipant got a job and no longer had time to participate.10

Baseline characteristics

CharacteristicN-acetylcysteine + Cognitive Behavioral TherapyTotalPlacebo + Cognitive Behavioral Therapy
Age, Continuous52.99 Years
STANDARD_DEVIATION 11.51
50.85 Years
STANDARD_DEVIATION 11.92
49.13 Years
STANDARD_DEVIATION 13.23
Ethnicity (NIH/OMB)
Hispanic or Latino
3 Participants4 Participants1 Participants
Ethnicity (NIH/OMB)
Not Hispanic or Latino
46 Participants86 Participants40 Participants
Ethnicity (NIH/OMB)
Unknown or Not Reported
0 Participants0 Participants0 Participants
Race (NIH/OMB)
American Indian or Alaska Native
0 Participants0 Participants0 Participants
Race (NIH/OMB)
Asian
0 Participants0 Participants0 Participants
Race (NIH/OMB)
Black or African American
26 Participants46 Participants20 Participants
Race (NIH/OMB)
More than one race
0 Participants0 Participants0 Participants
Race (NIH/OMB)
Native Hawaiian or Other Pacific Islander
0 Participants0 Participants0 Participants
Race (NIH/OMB)
Unknown or Not Reported
3 Participants3 Participants0 Participants
Race (NIH/OMB)
White
20 Participants41 Participants21 Participants
Region of Enrollment
United States
49 participants90 participants41 participants
Sex: Female, Male
Female
5 Participants7 Participants2 Participants
Sex: Female, Male
Male
44 Participants83 Participants39 Participants

Adverse events

Event typeEG000
affected / at risk
EG001
affected / at risk
deaths
Total, all-cause mortality
0 / 490 / 41
other
Total, other adverse events
30 / 4928 / 41
serious
Total, serious adverse events
3 / 492 / 41

Outcome results

Primary

Change in Alcohol Craving

Change in Alcohol craving as measured by change in Obsessive Compulsive Drinking Scale (OCDS) Total Score. Greater change/reduction in score indicates better outcomes and reduced alcohol craving. (Scores range from 0 to 56)

Time frame: From baseline to week 8

Population: 39 participants completed survey in NAC group and 37 participants completed survey in placebo group

ArmMeasureValue (MEAN)Dispersion
N-acetylcysteine (NAC) and Cognitive Behavioral Therapy (CBT)Change in Alcohol Craving-3.97 score on a scaleStandard Deviation 7.26
Placebo and Cognitive Behavioral Therapy (CBT)Change in Alcohol Craving-2.92 score on a scaleStandard Deviation 5.97
Primary

Change in Alcohol Use Disorder Severity

Change in Alcohol Use Disorder Severity as measured by change in average drinking days per week from baseline to week 8. Greater reduction in drinking days indicates better treatment outcomes. Drinking days measured over 1 week periods (7 days). Scale ranges from 0 days to 7 days.

Time frame: From baseline to week 8 of treatment

ArmMeasureValue (MEAN)Dispersion
N-acetylcysteine (NAC) and Cognitive Behavioral Therapy (CBT)Change in Alcohol Use Disorder Severity-2.65 drinking days reductionStandard Deviation 3.85
Placebo and Cognitive Behavioral Therapy (CBT)Change in Alcohol Use Disorder Severity-2.82 drinking days reductionStandard Deviation 4.86
Primary

Change in Post Traumatic Stress Disorder Severity

Change in post traumatic stress disorder severity as measured by Change in Clinician Administered PTSD Scale (CAPS-5) score from baseline to week 8. Greater change/reduction in score indicates better outcomes and greater reduction in PTSD symptomatology. (minimum score of 0 = absent to a maximum score of 80 = extreme)

Time frame: From baseline to week 8

ArmMeasureValue (MEAN)Dispersion
N-acetylcysteine (NAC) and Cognitive Behavioral Therapy (CBT)Change in Post Traumatic Stress Disorder Severity-6.93 score on a scaleStandard Deviation 13.42
Placebo and Cognitive Behavioral Therapy (CBT)Change in Post Traumatic Stress Disorder Severity-5.53 score on a scaleStandard Deviation 11.1
Primary

Change in Post Traumatic Stress Disorder Severity

Post traumatic stress disorder symptoms as measured by change/reduction in score of post traumatic stress disorder checklist (PCL-5) from baseline to week 8. Greater reduction in score indicates better treatment outcomes. (minimum score of 0 = absent to a maximum score of 80 = extreme)

Time frame: From baseline to week 8

Population: 39 participants completed survey in NAC group, and 37 completed survey in placebo group

ArmMeasureValue (MEAN)Dispersion
N-acetylcysteine (NAC) and Cognitive Behavioral Therapy (CBT)Change in Post Traumatic Stress Disorder Severity-12.97 score on a scaleStandard Deviation 18.36
Placebo and Cognitive Behavioral Therapy (CBT)Change in Post Traumatic Stress Disorder Severity-9.97 score on a scaleStandard Deviation 16.75

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026