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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT00548470
Other study ID # 06I/C34-0
Secondary ID
Status Completed
Phase Phase 4
First received
Last updated
Start date June 2007
Est. completion date December 2010

Study information

Verified date October 2017
Source Nathan Kline Institute for Psychiatric Research
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

This is an open label pre-post study of the effects of clinical treatment with varenicline on 1) decreasing smoking in schizophrenic patients, 2) improving selected cognitive measures in schizophrenic patients, and 3) psychopathology in schizophrenic patients. Patients are assessed on subjective and objective measures of smoking, selected cognitive measures, and special chemical measures, during baseline testing and during 8 weeks of treatment with varenicline (1-2 mg/day).


Recruitment information / eligibility

Status Completed
Enrollment 14
Est. completion date December 2010
Est. primary completion date September 2009
Accepts healthy volunteers No
Gender All
Age group 18 Years to 65 Years
Eligibility Inclusion Criteria:

- Clinical Diagnosis of Schizophrenia or Schizoaffective Psychosis

- Recent History of Cigarette smoking

- Ages 18-65

Study Design


Related Conditions & MeSH terms


Intervention

Drug:
Varenicline
Varenicline 1-2 mg/day

Locations

Country Name City State
United States Manhattan Psychiatric Center New York New York

Sponsors (2)

Lead Sponsor Collaborator
Nathan Kline Institute for Psychiatric Research University of Illinois at Chicago

Country where clinical trial is conducted

United States, 

References & Publications (1)

Smith RC, Lindenmayer JP, Davis JM, Cornwell J, Noth K, Gupta S, Sershen H, Lajtha A. Cognitive and antismoking effects of varenicline in patients with schizophrenia or schizoaffective disorder. Schizophr Res. 2009 May;110(1-3):149-55. doi: 10.1016/j.schr — View Citation

Outcome

Type Measure Description Time frame Safety issue
Primary Self Report of Smoking Patients self-report of smoking cigarettes. Patients were interviewed weekly about the number of cigarettes smoked. Number of cigarettes smoked in the past week. Baseline and during 2 months of treatment
Primary CO (Carbon Monoxide) Breathalyzer Level Carbon Monoxide in breath ,parts per million baseline and during 2 months of treatment
Primary Plasma Cotinine cotinine level in plasma ng/ml. baseline 1 month and 2 months
Secondary RBANS Neuropsychological Battery The scale is Repeatable Battery for the Assessment to Neuropsychological Status (RBANS). This scale measures cognitive function in patients with schizophrenia. RBANS scores for list learning range from 0 to 40. RBANS Index scores for visual-spatial index, language index, and Total score range from 40-160. RBANS Total score is the sum of score of all the individual items ( items 1-12) on the RBANS scale. List Learning scores range from 0 to 40. Visual Spatial Construction index scores range from 0 to 30.. Higher scores on all these measures indicate better performance or better cognitive ability. baseline and month 2 of treatment
Secondary Change From Baseline in Psychiatric Symptoms The Positive and Negative Syndrome Scale (PANSS) was used to measure psychiatric symptoms. Item scores ranged from 1 (Absent) to 6 (Severe) for symptoms on the Positive Scale (total subscale range: 7-42), the Negative Scale (total subscale range: 7-42), and the General Psychopathology Scale (total subscale range:16-96). All three subscales were summed for the PANSS total score (total scale range: 30-180). Higher numbers indicate more psychopathology. Therefore, if scores are reduced at post-baseline ratings, this would indicate lower psychopathology. Baseline and 2 months later
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