The CAMPUS Project: Cholinergic Augmentation of Cognitive Deficits in Schizophrenia

Schizophrenia Clinical Trial

Official title:

PHARMACOLOGICAL TREATMENT OF COGNITIVE DEFICITS IN SCHIZOPHRENIC PATIENTS: The Effects of Central Cholinergic Augmentation on Cognitive Deficits and Psychopathology

Clinical Trial Details — Status: Terminated

Administrative data

• NCT number: NCT00206947
• Other study ID #: 363051
• Secondary ID: KF 02-033/02DMA
• Status: Terminated
• Phase: Phase 2
• First received: September 11, 2005
• Last updated: September 19, 2011
• Start date: December 2002
• Est. completion date: January 2005

Study information

• Verified date: July 2008
• Source: University of Copenhagen
• Contact: n/a
• Is FDA regulated: No
• Health authority: Denmark: National Board of Health
• Study type: Interventional

Clinical Trial Summary

The present study will specify and delineate the separate components of cognitive deficits and examine the effects of adjunctive cholinergic augmentation on these cognitive deficits as well as psychopathology in schizophrenic patients treated with an antipsychotic compound with no aberrant binding affinity for the cholinergic receptor system. The hypothesis is that cholinergic augmentation using donepezil will improve cognitive deficits, sensory gating deficits, and psychopathology in schizophrenic patients treated with an atypical antipsychotic (ziprasidone).

Description:

The purpose of the study was to examine the effects of cholinergic augmentation of atypical antipsychotic medication on:

• Cognitive deficits

• Sensorimotor gating

• Psychopathology

The primary objective was to examine:

• The effects of donepezil, compared to the effects of placebo, on cognitive function, sensorimotor gating and psychopathology in patients treated with an atypical antipsychotic (ziprasidone).

Secondary objectives are to examine:

• The effect of donepezil, compared to the effects of placebo, on cognitive function, sensorimotor gating and psychopathology in patients treated with ziprasidone.

• Which specific areas of cognitive deficits benefit from cholinergic augmentation of atypical antipsychotic treatment.

• The interactions between cognitive deficits and psychopathology: To what extent the effects of cholinergic augmentation on psychopathology, sensorimotor gating, and cognition are independent or correlated.

• Which specific brain areas are activated during cholinergic augmentation of treatment with an atypical antipsychotic drug (ziprasidone).

Participants: Schizophrenic men and women between the ages 18 to 55 who meet the ICD-10 criteria for schizophrenia living in the catchment area of the psychiatric departments of Bispebjerg University Hospital,Rigshospitalet, or Psychiatric Center, Glostrup. Patients can be either unmedicated, or need to be switched from other antipsychotic medications due to side-effects, or lack of effect on negative symptoms, positive symptoms, or cognitive function. Patients can be enrolled in the study as inpatients or outpatients, and changes in hospitalization status during the trial are allowed. Patients were stabilized on antipsychotic medication (ziprasidone) before they were randomized to treatment with either donepezil or placebo.

Recruitment information / eligibility

• Status: Terminated
• Enrollment: 50
• Est. completion date: January 2005
• Est. primary completion date: January 2005
• Accepts healthy volunteers: Accepts Healthy Volunteers
• Gender: Both
• Age group: 18 Years to 55 Years

Eligibility

Inclusion Criteria:

• Patients: Men and women between the ages 18 to 55 who meet the ICD-10 criteria for schizophrenia living in the catchment area of the psychiatric departments of Bispebjerg University Hospital, Psychiatric Center, Glostrup and Rigshospitalet. Patients can be either unmedicated, or need to be switched from other antipsychotic medications due to side-effects, or lack of effect on negative symptoms, positive symptoms, or cognitive function.

• Controls: Healthy men and women matched according to gender, age, and socio-economic status (determined by the level of education and income of parents).

Exclusion Criteria:

• Patients: Patients hospitalized against their will. Patients with a serious medical illness or with laboratory abnormalities, where pharmacotherapy poses a substantial clinical risk; pregnant or lactating patients; patients with organic psychosis, a history of severe head trauma or convulsive disorders, or patients with mental retardation. Patients with significant alcohol- or drug dependence are excluded.

• Controls: Pregnant or lactating women; a history of severe head trauma; mental retardation; learning difficulties; a history of psychiatric illness or a familial predisposition to psychiatric illness (in first-degree relatives); significant alcohol- or drug dependence; episodic incidents of excessive alcohol consumption or drug abuse are not reasons for exclusion. Abuse is monitored by interviewing patients and by measuring the urine content for amphetamine, cannabinoles, opiates, and benzodiazepines. Concomitant use of benzodiazepines for agitation or insomnia (oxazepam up to 45 mg daily) is allowed when needed and when used conservatively during the trial. Use of anticholinergic compounds is not allowed.

Study Design

Allocation: Randomized, Endpoint Classification: Efficacy Study, Intervention Model: Parallel Assignment, Masking: Double Blind (Subject, Caregiver, Investigator, Outcomes Assessor), Primary Purpose: Treatment

Related Conditions & MeSH terms

• Cognition Disorders
• Schizophrenia

Intervention

Drug:
• donepezil (5-10 mg/day)
Donepezil will be administered in a dose optimized for treatment, to patients who are stabilized on a ziprasidone treatment
• Placebo
Placebo will be added to the medication of schizophrenia patients who are first stabilized on a ziprasidone treatment

Locations

Country	Name	City	State
Denmark	Dept. of Psychiatry O, Rigshospitalet, Blegdamsvej 9	Copenhagen
Denmark	Center for Neuropsychiatric Schizophrenia Research, University of Copenhagen, Dept. F, Bispebjerg Hospital	Copenhagen NV
Denmark	Psychiatric Center, Glostrup	Glostrup
Denmark	Danish Research Center for Magnetic Resonance Imaging, Hvidovre Hospital	Hvidovre

Sponsors (4)

Lead Sponsor	Collaborator
Birte Glenthoj	Glostrup University Hospital, Copenhagen, Pfizer, Rigshospitalet, Denmark

Country where clinical trial is conducted

Denmark, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	PANSS (Positive and Negative Symptom Scale)		baseline and after treatment	No
Primary	the CGI (Clinical Global Impression scale)		baseline and after treatment	No
Primary	the ESRS (Extrapyramidal Symptom Rating Scale)		baseline and after treatment	No
Primary	Cognitive functions: A comprehensive test battery focuses on central cognitive deficits in schizophrenia: i.e. memory functions, attention, executive functions, reaction time, as well as pre-morbid and current intelligence.		baseline and after treatment	No
Secondary	MRI		baseline and after treatment	No
Secondary	fMRI		baseline and after treatment	No

External Links

•   Center for Neuropsychiatric Schizophrenia Research (CNSR)