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N/A Completed N=28 Randomized Double-blind Treatment

A Pilot Trial of Acute N-Acetylcysteine Effects on Working Memory and Other Cognitive Functions in Schizophrenia

Source: ClinicalTrials.gov NCT01232790 ↗
Enrolled (actual)
28
Serious AEs
0.0%
Results posted
Apr 2014
Primary outcomePrimary: BACS Composite RAW Score — 229.04; 227.83 units on a scale

Summary

The purpose of this study is to evaluate the effects of the amino acid supplement N-Acetylcysteine versus placebo on working memory and other cognitive functions in persons with a diagnosis of schizophrenia.

Outcome Measures

OutcomeResultp-value
PRIMARY
BACS Composite RAW Score
238.55; 239.33 —
SECONDARY
Letter/Number Sequencing Task Tests for Attention, Concentration & Mental Control (LNS) RAW SCORE.
14.27; 14.44 —
SECONDARY
Brief Visuospatial Memory Test (BVMT) RAW SCORE.
18.82; 17.44 —
SECONDARY
Brief Psychiatric Rating Scale (BPRS)Total Score
1.70; 0.89 —

Eligibility Criteria

Inclusion Criteria

  • Subjects will be between 18-60
  • Meet Diagnostic and Statistical Manual-IV (DSM) criteria for schizophrenia
  • Be on a stable dose of antipsychotic medication for at least 1 month
  • Be deemed clinically stable for 3 months by the regular clinical staff

Exclusion Criteria

  • Current substance or alcohol abuse
  • Pregnancy
  • Clozapine treatment
  • Known sensitivity to sulphur containing compounds
  • Previous diagnosis of mental retardation
  • Nitroglycerin use
  • Asthma diagnosis, verified and treated by a primary care doctor
  • Use of any other medication that may interact with the study medication
View full record on ClinicalTrials.gov →

Data sourced from ClinicalTrials.gov (NCT01232790). Outcome figures and adverse-event rates are extracted automatically from the registry's posted results and are provided for clinician reference, not as a substitute for the primary publication. Informational only — not medical advice.

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