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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT00588731
Other study ID # 0710003164
Secondary ID 07TGS-1082
Status Completed
Phase Phase 2
First received December 29, 2007
Last updated June 6, 2017
Start date February 2009
Est. completion date December 2013

Study information

Verified date June 2017
Source Yale University
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

This study is a six-week, randomized, placebo-controlled, fixed dose trial comparing cannabidiol Vs. placebo added to a stable dose of antipsychotic medications in patients diagnosed with schizophrenia.


Recruitment information / eligibility

Status Completed
Enrollment 41
Est. completion date December 2013
Est. primary completion date December 2013
Accepts healthy volunteers No
Gender All
Age group 18 Years to 65 Years
Eligibility Inclusion Criteria:

- Schizophrenia or Schizoaffective disorder (DSM-IV SCID-confirmed),

Exclusion Criteria:

- Women who are pregnant, nursing or unwilling to use appropriate birth control measures during study participation.

Study Design


Intervention

Drug:
Cannabidiol
Active Cannabidiol daily over 6 weeks
Placebo
Placebo

Locations

Country Name City State
United States Yale University New Haven Connecticut

Sponsors (2)

Lead Sponsor Collaborator
Yale University Stanley Medical Research Institute

Country where clinical trial is conducted

United States, 

Outcome

Type Measure Description Time frame Safety issue
Primary Verbal Short Term Memory Verbal short term memory is measured through the Hopkins Verbal Learning Test. Each trial has a max total score of 12 (range of 0-12), and the max total score for all three trials is 36 (range of 0-36). However, the data listed below is reported in the form of a t-score, with a higher score representing better verbal learning. These t-score values are normalizing the scores to populations, comparing them to a representative sample, with a mean of 50. 6 weeks
Secondary Overall Cognition as Measured on the MATRICS Battery Measurement and Treatment Research to Improve Cognition in Schizophrenia (MATRICS) Consensus Cognitive Battery (MCCB) is intended to provide a relatively brief evaluation of key cognitive domains relevant to schizophrenia and related disorders. A higher score indicates better cognition (i.e. speed of processing, attention, verbal and non-verbal working memory, visual learning, reasoning, problem solving, and social cognition). The below scores are t-score values, which are normalized scores to the population and comparing the scores to a representative sample. 6 weeks
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