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Phase 4 Completed N=38 Randomized Quadruple-blind Treatment

Effects of Weekly Dosing of D-cycloserine on Cognitive Function in Individuals With Schizophrenia

Source: ClinicalTrials.gov NCT00455702 ↗
Enrolled (actual)
38
Serious AEs
2.6%
Results posted
Aug 2014
Primary outcomePrimary: Main Outcome Measure: The Change From Baseline to Week 8 on the SANS — 2.06; -2.11 Units on a scale

Summary

The study aims to assess the effects of single dose and repeated weekly dosing of 50mg d-cycloserine versus placebo on cognitive and memory functioning in schizophrenia patients. The study will also examine the effects of 50mg d-cycloserine on positive symptoms and negative symptoms, as well as assess tolerability and side-effects.

Outcome Measures

OutcomeResultp-value
PRIMARY
Main Outcome Measure: The Change From Baseline to Week 8 on the SANS
2.06; -2.11
SECONDARY
Treatment Effects on the Positive Syndrome Subscale of the PANSS
.19; -.19

Eligibility Criteria

Inclusion Criteria

  • Male or female
  • Age 18-65 years
  • Diagnosis of schizophrenia or schizoaffective disorder, depressed type
  • Stable dose of antipsychotic for at least 4 weeks.
  • Able to provide informed consent
  • Able to complete a cognitive battery

Exclusion Criteria

  • Current treatment with clozapine
  • Dementia
  • Seizure disorder
  • Unstable medical illness
  • Active substance abuse
  • Pregnancy, nursing, or unwilling to use appropriate birth control measures during participation if female and fertile.
View full record on ClinicalTrials.gov →

Data sourced from ClinicalTrials.gov (NCT00455702). 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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