N-acetylcysteine in the Treatment of PTSD and Addiction (NAC)
PTSD, Addiction
About this trial
This is an interventional treatment trial for PTSD
Eligibility Criteria
Inclusion Criteria:
- 18-65 year old
- U.S. military Veteran, Reservist, or National Guard member
- DSM-IV diagnostic criteria for current (past 6 months) SUD and PTSD or subthreshold PTSD (i.e., met criteria for cluster B (re-experiencing) and either cluster C (avoidance) or D (hyperarousal), as well as duration of one month and clinically significant impairment)
- Score of > 21 on the Mini-Mental State Exam (MMSE).
Exclusion Criteria:
- Unstable medical conditions
- Bipolar or psychotic disorders
- Seizures or asthma
- Prior treatment with NAC
- Suicidality
- Enrolled in ongoing PTSD treatment (pharmacotherapy or psychosocial)
- Females: could not be pregnant or lactating
Sites / Locations
Arms of the Study
Arm 1
Arm 2
Experimental
Placebo Comparator
N-Acetylcysteine
Placebo
Eligible participants were randomized to either NAC (2400 mg/day) or placebo for 8 weeks. The starting dose of NAC was 1200 mg twice daily (2400 mg/day). All NAC and placebo capsules contained riboflavin 25 mg, which was used as a biomarker for medication compliance.
Identical appearing placebo capsules were dispensed. All NAC and placebo capsules contained riboflavin 25 mg, which was used as a biomarker for medication compliance. Study medications (USP-grade NAC and matched placebo capsules) dispensed to participants by the medical clinician or study staff. Treatment assignment followed a pre-arranged randomization scheme and was carried out by study personnel at the pharmacy (i.e., personnel not involved in clinical management of participants to preserve the double-blind design).