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The Effects of Varenicline on Cognitive Function in Patients With Schizophrenia

Primary Purpose

Schizophrenia

Status
Completed
Phase
Phase 3
Locations
Korea, Republic of
Study Type
Interventional
Intervention
Varenicline(Chantix)
Placebo
Sponsored by
Inje University
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Schizophrenia focused on measuring Schizophrenia, Cognition, Varenicline

Eligibility Criteria

18 Years - 60 Years (Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • Clinically stable patients with schizophrenia

Exclusion Criteria:

  • Refractory schizophrenia
  • Mental Retardation
  • Serious Medical illness

Sites / Locations

  • Dongrae Hospital
  • Jamyeong
  • Busan Paik Hospital
  • Ahab Hospital
  • Dongseo hospital

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

Placebo Comparator

Arm Label

Varenicline

Placebo

Arm Description

The effect of varenicline on cognitive function of Varenicline(Chantix) is being compared to that of placebo

The effect of placebo comparator is being compared to that of varenicline

Outcomes

Primary Outcome Measures

To examine the effects of varenicline treatment used concomitantly with antipsychotic medications, on cognitive dysfunction in people with schizophrenia.

Secondary Outcome Measures

To evaluate the effect of this combination therapy on smoking in people with schizophrenia.

Full Information

First Posted
August 30, 2007
Last Updated
August 3, 2009
Sponsor
Inje University
Collaborators
Stanley Medical Research Institute
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1. Study Identification

Unique Protocol Identification Number
NCT00523445
Brief Title
The Effects of Varenicline on Cognitive Function in Patients With Schizophrenia
Official Title
Varenicline, an Alpha 4 Beta 2 Nicotinic Acetylcholine Receptor Partial Agonist, on Cognitive Dysfunction in 120 Patients With Schizophrenia: a Randomized, Double Blind, 8 Weeks Trial
Study Type
Interventional

2. Study Status

Record Verification Date
August 2009
Overall Recruitment Status
Completed
Study Start Date
September 2007 (undefined)
Primary Completion Date
June 2009 (Actual)
Study Completion Date
July 2009 (Actual)

3. Sponsor/Collaborators

Name of the Sponsor
Inje University
Collaborators
Stanley Medical Research Institute

4. Oversight

Data Monitoring Committee
Yes

5. Study Description

Brief Summary
The primary objective of this project is to examine the effects of varenicline treatment used concomitantly with antipsychotic medications, on cognitive dysfunction in people with schizophrenia. The secondary objective is to evaluate the effect of this combination therapy on smoking in people with schizophrenia. This study will be a randomized, double blind, parallel group, placebo controlled 8 weeks trial.
Detailed Description
Cognitive deficits have been considered as a core symptom domain of schizophrenia. Amelioration of or improvement in cognitive impairments is becoming an important focus of clinical treatment development. Varenicline is a potent and selective alpha 4 beta 2 nicotinic acetylcholine receptor partial agonist that has been developed for smoking cessation. In animal studies, alpha 4 beta 2 receptor agonists significantly improve working memory and attention function. Subjects will be assigned in 1:1 ratio to receive varenicline or placebo respectively. Assessments will be done using several neuropsychologic tests, clinical rating scale including assessment of nicotine withdrawal scales.Varenicline has been found to be efficacious for smoking cessation in the general population and animal studies have demonstrated the cognitive benefits of this agent. However, no published work is available evaluating the cognitive effects in humans. Thus, patients may experience improvements in cognitive function and in people who are smokers, these people may be able to achieve abstinence in smoking. This will in turn improve long-term functional outcomes and health outcomes in people with schizophrenia. This is an exciting opportunity for discovery if indeed cognitive abilities could be improved with this adjunctive treatment.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Schizophrenia
Keywords
Schizophrenia, Cognition, Varenicline

7. Study Design

Primary Purpose
Treatment
Study Phase
Phase 3
Interventional Study Model
Parallel Assignment
Masking
ParticipantInvestigator
Allocation
Randomized
Enrollment
120 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
Varenicline
Arm Type
Experimental
Arm Description
The effect of varenicline on cognitive function of Varenicline(Chantix) is being compared to that of placebo
Arm Title
Placebo
Arm Type
Placebo Comparator
Arm Description
The effect of placebo comparator is being compared to that of varenicline
Intervention Type
Drug
Intervention Name(s)
Varenicline(Chantix)
Intervention Description
The dose of antipsychotic drug will remain fixed throughout the study and the titration of varenicline will be as follows: varenicline 0.5 mg/d for days 1 to 3, 0.5 mg twice per day for days 4 to 7, then 1 mg twice per day through week 8.
Intervention Type
Drug
Intervention Name(s)
Placebo
Intervention Description
The dose of antipsychotic and concomitant medications remained fixed throughout the study and the titration of varenicline was as follows: Placebo will be supplied twice daily through week 8.
Primary Outcome Measure Information:
Title
To examine the effects of varenicline treatment used concomitantly with antipsychotic medications, on cognitive dysfunction in people with schizophrenia.
Time Frame
8 weeks
Secondary Outcome Measure Information:
Title
To evaluate the effect of this combination therapy on smoking in people with schizophrenia.
Time Frame
8 weeks

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
60 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Clinically stable patients with schizophrenia Exclusion Criteria: Refractory schizophrenia Mental Retardation Serious Medical illness
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Joo-Cheol Shim, MD.PhD
Organizational Affiliation
Inje University
Official's Role
Principal Investigator
Facility Information:
Facility Name
Dongrae Hospital
City
Busan
ZIP/Postal Code
609-370
Country
Korea, Republic of
Facility Name
Jamyeong
City
Busan
ZIP/Postal Code
612-827
Country
Korea, Republic of
Facility Name
Busan Paik Hospital
City
Busan
ZIP/Postal Code
614-735
Country
Korea, Republic of
Facility Name
Ahab Hospital
City
BUsan
ZIP/Postal Code
616-824
Country
Korea, Republic of
Facility Name
Dongseo hospital
City
Masan
ZIP/Postal Code
630-856
Country
Korea, Republic of

12. IPD Sharing Statement

Citations:
PubMed Identifier
27543252
Citation
Jeon DW, Shim JC, Kong BG, Moon JJ, Seo YS, Kim SJ, Oh MK, Jung DU. Adjunctive varenicline treatment for smoking reduction in patients with schizophrenia: A randomized double-blind placebo-controlled trial. Schizophr Res. 2016 Oct;176(2-3):206-211. doi: 10.1016/j.schres.2016.08.016. Epub 2016 Aug 16.
Results Reference
derived
PubMed Identifier
22048460
Citation
Shim JC, Jung DU, Jung SS, Seo YS, Cho DM, Lee JH, Lee SW, Kong BG, Kang JW, Oh MK, Kim SD, McMahon RP, Kelly DL. Adjunctive varenicline treatment with antipsychotic medications for cognitive impairments in people with schizophrenia: a randomized double-blind placebo-controlled trial. Neuropsychopharmacology. 2012 Feb;37(3):660-8. doi: 10.1038/npp.2011.238. Epub 2011 Nov 2.
Results Reference
derived

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The Effects of Varenicline on Cognitive Function in Patients With Schizophrenia

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