Efficacy Study on Cognitive Functions in Schizophrenic Patients

NCT ID: NCT00761670

Last Updated: 2010-12-09

Basic Information

• Recruitment Status: COMPLETED
• Clinical Phase: PHASE4
• Total Enrollment: 37 participants
• Study Classification: INTERVENTIONAL
• Study Start Date: 2008-09-30
• Study Completion Date: 2010-01-31

Brief Summary

Primary objectives

• To compare neurocognitive effects of amisulpride with those of risperidone in patients with chronic schizophrenia, as assessed by the general cognitive index, a measure of overall cognitive functioning in schizophrenia

Secondary objectives

• Secondary analyses will be conducted to determine how the two atypical agents' neurocognitive effects compare with regard to their profile of therapeutic action (based on individual cognitive domain scores in seven cognitive domains, including speed of processing, attention/vigilance, working memory, verbal learning and memory, visual learning and memory, reasoning and problem solving and social cognition);
• Investigate whether amisulpride elicits more improvement on negative symptoms compared to risperidone treatment, as measured by the total score on the Scale of the Assessment of Negative Symptoms (SANS) 8 and by the Negative Symptom Subscale of the Positive and Negative Symptom Scale (PANSS);
• Assess whether amisulpride improves overall functioning and individual domains of psychotic symptoms compared to risperidone as measured by the Clinical Global Impression (CGI), and the total and positive and general psychopathology subscale scores of PANSS and by the individual domains of SANS, respectively;
• Evaluate the safety and tolerability of amisulpride and risperidone based on the study completion rates, and frequency of abnormal laboratory values, prolactin serum concentrations and on the Simpson Angus Scale for Extrapyramidal Symptoms (SAS) 10 and the Abnormal Involuntary Movement Scale (AIMS).

Conditions

Schizophrenia

Study Design

• Allocation Method: RANDOMIZED
• Intervention Model: PARALLEL
• Primary Study Purpose: TREATMENT
• Blinding Strategy: NONE

Study Groups

1

Group Type: ACTIVE_COMPARATOR

amisulpride and risperidone

Intervention Type: DRUG

amisulpride tablet 400-800 mg/day risperidone tablet 4-8 mg/day

2

Group Type: ACTIVE_COMPARATOR

amisulpride and risperidone

Intervention Type: DRUG

amisulpride tablet 400-800 mg/day risperidone tablet 4-8 mg/day

Interventions

amisulpride and risperidone

amisulpride tablet 400-800 mg/day risperidone tablet 4-8 mg/day

Intervention Type: DRUG

Eligibility Criteria

Inclusion Criteria

• Diagnosis: DSM-IV schizophrenia (any subtype)
• Duration of illness: ≥ 5 years
• Concomitant standing or prn medications (except other antipsychotics and those contraindicated in the respective package inserts [amisulpride or risperidone]) are permitted during treatment phase, if they were present at a stable dose for at least 6 weeks prior to the start of initial treatment with study medication
• Overall symptom severity: patients must evidence a total score of 60 or higher on the PANSS scale
• Clinical Symptoms: A score of 4 (moderate) or greater on any of the 7 items of the PANSS Positive Symptom Subscale is present
• Cognitive status (minimum performance level): subject must be able to validly complete the baseline MATRICS assessment
• Clinical judgment by the investigator that treatments with amisulpride or risperidone are warranted due to suboptimal clinical outcome despite previous treatments

Exclusion Criteria

• Past or current intolerance of amisulpride or risperidone side effects that are judged by the investigator to be unsafe, dose-limiting, or likely to result in study discontinuation.
• Any contraindication for amisulpride or risperidone therapy as indicated in the drug description.
• Presence of any unstable or untreated medical disorder.
• Any history of seizures or seizure disorder other than febrile seizures of childhood;
• History of positive hepatitis B surface antigen.
• Any abnormal laboratory test that is judged to be clinically significant by the investigator.
• A history of significant head injury/trauma, as defined by:

A. loss of consciousness (LOC) for more than 1 hour B. recurring seizures resulting from the head injury C. clear cognitive sequelae of the injury D. cognitive rehabilitation following the injury

• Alcohol or substance dependence within the past 12 months or abuse within the past 3 months. Any subject with positive urine toxicology or alcohol use that is considered abnormal at baseline.
• Clinically significant suicidal or homicidal behavior or attempts within past 6 months.
• Pregnant or breast-feeding women
• Absence of medically approved contraceptive methods for female of childbearing potential.

The above information is not intended to contain all considerations relevant to a patient's potential participation in a clinical trial.

• Minimum Eligible Age: 18 Years
• Maximum Eligible Age: 65 Years
• Eligible Sex: ALL
• Accepts Healthy Volunteers: No

Sponsors

Sanofi

INDUSTRY

Sponsor Role: lead

Responsible Party

sanofi-aventis

Principal Investigators

László Erős, MD

Role: STUDY_DIRECTOR

sanofi-aventis Hungary

Locations

Sanofi-Aventis Administrative Office

Budapest, , Hungary

Countries

Hungary

Other Identifiers

EudraCT #: 2007-005772-13

Identifier Type: -

Identifier Source: secondary_id

AMISU_L_01008

Identifier Type: -

Identifier Source: org_study_id