drugset / Trial / NCT01664260

Efficacy Mechanism of N-acetylcysteine in Patients With Posttraumatic Stress Disorder

NCT01664260

Phase 2 Withdrawn Ewha Womans University
RandomizedParallel-groupQuadruple-blindTreatment

Summary

It has been suggested that N-acetylcysteine exerts neuroprotective effects by regulating neurotransmitters and cell signaling pathways. We hypothesize that oral N-acetylcysteine augmentation will help reduce symptoms in patients with posttraumatic stress disorder as well as improve cognitive functions. We also expect that the N-acetylcysteine augmentation will induce change in structural, functional, and neurochemical aspects of the brain. In this study, we plan to conduct a randomized, double-blind, placebo-controlled augmentation study with N-acetylcysteine in addition to escitalopram. We will assess the efficacy and safety of the N-acetylcysteine augmentation.

Timeline

Start
2012-11-01
Primary completion
2016-12-01
Completion
2016-12-31

Drugs

EvaluationDrugModalityDoseRoute
Subject N-acetylcysteine Small molecule 1200 mg Oral