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Efficacy and Tolerability of Switching to Ziprasidone From Other Antipsychotics

Primary Purpose

Schizophrenia, Schizoaffective Disorder

Status
Completed
Phase
Phase 4
Locations
United States
Study Type
Interventional
Intervention
ziprasidone
Sponsored by
Bronx Psychiatric Center
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

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

Eligibility Criteria

18 Years - 65 Years (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • Schizophrenia or schizoaffective
  • Capacity to give consent
  • Stable, on the same medication for a month but only partial response or with unacceptable side effects 18-65 years of age

Exclusion Criteria:

  • Repeated non-compliance
  • Current depot medication
  • Active medical conditions
  • QTc >500msec
  • Previous non-response
  • Previous treatment with ziprasidone

Sites / Locations

  • Bronx Psychiatric Center
  • Buffalo Psychiatric Center

Arms of the Study

Arm 1

Arm Type

Experimental

Arm Label

Experimental

Arm Description

Open label change to ziprasidone

Outcomes

Primary Outcome Measures

Positive and Negative Syndrome Scale (PANSS) Measuring Symptoms of Schizophrenia
Minimum score 32 (best) maximum 210 (worst)

Secondary Outcome Measures

Clinical Global Impression (CGI) Scores the Evaluator's Overall Impression of Severity (CGI-S) or Change (CGI-I) in Illness.
CGI-S scores from 1 = normal to 7 = most extremely ill
Weight
Fasting Glucose
Amount of glucose in the blood in mg/dl
Cholesterol
Abnormal Involuntary Movement Scale (AIMS) Measures Tardive Dyskinesia
Scores 0 (none) to 4 (severe) choreo-athetoid and dystonic movements of seven parts of the body with a maximum score 28
Simpson-Angus Scale Measures Drug Induced Parkinsonism
Measures 10 signs, (not all of which are now considered Parkinsonism), minimum score 0 (no Parkinsonism) maximum 40.
Corrected QT Interval (QTc)
Time interval between Q and T waves on EKG corrected for pulse rate. Over 500 msec may be dangerous
Brief Assessment of Cognition in Schizophrenia (BACS)
Scores on the BACS scale, which measures cognition, were changed to Z-scores based on normal controls from Keefe (2008) A Z-score of zero would indicate cognition the same as the normal controls. Negative scores indicate cognition worse than the normal. Theoretically there are no maximum or minimum scores.
Calgary Depression Scale for Schizophrenia
Score on scale, from 0 to 27, above 6 considered indicative of depression, higher scores mean worse outcome,
Personal Evaluation of Transitions in Treatment Scale (PETiTP
PETiT is a 30 item self administered scale measuring response to and tolerability and adherence to antipsychotic medication in people with schizophrenia. The range is 30 to 100. Higher scores are better. Although different features are assessed there is a single total score - no subscales.
Medical Outcomes Study Cognitive Functioning Scale (MOS-COG)
MOS-COG measures day to day problems in six aspects of cognitive functioning. The scores are converted to 0-100 and so can range from 0 to 100 with 100 being the best. Population means are 70 to 80.
Barnes Akathisia Scale
Barnes Akathisia Scale measures akathisia: a score of zero is none (good) maximum score is 12
HbA1c
Lab measure of glycated hemoglobin indicative of blood glucose over the last three months. At that time in the US measured as a percentage (of glucose attached to hemoglobin). No maximum or minimum but over 6.5% is generally considered indicative of diabetes.
Insulin Level
Measure of the amount of insulin in the blood, in uIU/ml. No minimum or maximum but fasting levels are usually below 25 uIU/ml. After a dose of glucose they may be 30 to 230 uIU/ml.
Antipsychotic Medication Costs
No data were collected because it turned out we had no way of measuring the costs. No subjects were analysed by costs

Full Information

First Posted
April 6, 2007
Last Updated
April 22, 2020
Sponsor
Bronx Psychiatric Center
Collaborators
Pfizer, Buffalo Psychiatric Center, Rochester Psychiatric Center
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1. Study Identification

Unique Protocol Identification Number
NCT00458211
Brief Title
Efficacy and Tolerability of Switching to Ziprasidone From Other Antipsychotics
Official Title
Evaluation of Efficacy and Tolerability of Switching to Ziprasidone From Other Antipsychotic Medications
Study Type
Interventional

2. Study Status

Record Verification Date
April 2020
Overall Recruitment Status
Completed
Study Start Date
May 2005 (undefined)
Primary Completion Date
April 2008 (Actual)
Study Completion Date
April 2008 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Bronx Psychiatric Center
Collaborators
Pfizer, Buffalo Psychiatric Center, Rochester Psychiatric Center

4. Oversight

Data Monitoring Committee
No

5. Study Description

Brief Summary
Because ziprasidone has not been extensively studied and is not widely accepted in the severely mentally ill in State hospitals this study aims to demonstrate its effectiveness and relative lack of side effects. 75 patients with schizophrenia or schizoaffective disorder who need a change of medication because of ineffectiveness or side effects will be changed to ziprasidone and followed with detailed assessments for eight weeks. The hypothesis is that they will improve and have fewer side effects.
Detailed Description
Ziprasidone has been found in studies and practice to be efficacious and tolerated well but has not been well studied or well accepted in the very severely ill in State Hospitals. This study aims to fill that gap by examining 75 patients with schizophrenia or schizoaffective disorder who require a change of medication because of poor response or unacceptable side effects. After signing consent and having a baseline assessment they will, if necessary, be reduced to one antipsychotic then started on ziprasidone, increasing to 160mg the second day. The one antipsychotic they had been on will be reduced over a week and stopped. The ziprasidone can be increased to 240mg after three weeks if necessary. The study will last eight weeks with efficacy assessed by Clinical Global Impressions (CGI), Positive and Negative Syndrome Scale (PANSS) every two weeks and Brief Assessment of Cognition, Calgary Depression Scale for Schizophrenia, Personal Evaluation of Transitions in Treatment and Medical Outcomes Study Cognitive Questions at the beginning and end. Side effects will be measured by movement disorder scales (Simpson-Angus scale for Parkinsonism (SANRS), Abnormal Involuntary Movement Scale (AIMS) and Barnes Akathisia Scale (BAS)), ECG and weight and blood metabolic measures. The hypothesis is that ziprasidone will be generally effective and that side effects especially metabolic indices will be reduced.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Schizophrenia, Schizoaffective Disorder
Keywords
Schizophrenia, Ziprasidone

7. Study Design

Primary Purpose
Treatment
Study Phase
Phase 4
Interventional Study Model
Single Group Assignment
Masking
None (Open Label)
Allocation
N/A
Enrollment
40 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Experimental
Arm Type
Experimental
Arm Description
Open label change to ziprasidone
Intervention Type
Drug
Intervention Name(s)
ziprasidone
Intervention Description
Ziprasidone by mouth 40mg twice a day (bid) for one day, then 80mg bid; may be increased to 120mg bid after three weeks
Primary Outcome Measure Information:
Title
Positive and Negative Syndrome Scale (PANSS) Measuring Symptoms of Schizophrenia
Description
Minimum score 32 (best) maximum 210 (worst)
Time Frame
Baseline to 8 weeks
Secondary Outcome Measure Information:
Title
Clinical Global Impression (CGI) Scores the Evaluator's Overall Impression of Severity (CGI-S) or Change (CGI-I) in Illness.
Description
CGI-S scores from 1 = normal to 7 = most extremely ill
Time Frame
8 weeks
Title
Weight
Time Frame
8 weeks
Title
Fasting Glucose
Description
Amount of glucose in the blood in mg/dl
Time Frame
8 weeks
Title
Cholesterol
Time Frame
8 weeks
Title
Abnormal Involuntary Movement Scale (AIMS) Measures Tardive Dyskinesia
Description
Scores 0 (none) to 4 (severe) choreo-athetoid and dystonic movements of seven parts of the body with a maximum score 28
Time Frame
8 weeks
Title
Simpson-Angus Scale Measures Drug Induced Parkinsonism
Description
Measures 10 signs, (not all of which are now considered Parkinsonism), minimum score 0 (no Parkinsonism) maximum 40.
Time Frame
8 weeks
Title
Corrected QT Interval (QTc)
Description
Time interval between Q and T waves on EKG corrected for pulse rate. Over 500 msec may be dangerous
Time Frame
8 weeks
Title
Brief Assessment of Cognition in Schizophrenia (BACS)
Description
Scores on the BACS scale, which measures cognition, were changed to Z-scores based on normal controls from Keefe (2008) A Z-score of zero would indicate cognition the same as the normal controls. Negative scores indicate cognition worse than the normal. Theoretically there are no maximum or minimum scores.
Time Frame
8 weeks
Title
Calgary Depression Scale for Schizophrenia
Description
Score on scale, from 0 to 27, above 6 considered indicative of depression, higher scores mean worse outcome,
Time Frame
8 weeks
Title
Personal Evaluation of Transitions in Treatment Scale (PETiTP
Description
PETiT is a 30 item self administered scale measuring response to and tolerability and adherence to antipsychotic medication in people with schizophrenia. The range is 30 to 100. Higher scores are better. Although different features are assessed there is a single total score - no subscales.
Time Frame
8 weeks
Title
Medical Outcomes Study Cognitive Functioning Scale (MOS-COG)
Description
MOS-COG measures day to day problems in six aspects of cognitive functioning. The scores are converted to 0-100 and so can range from 0 to 100 with 100 being the best. Population means are 70 to 80.
Time Frame
8 weeks
Title
Barnes Akathisia Scale
Description
Barnes Akathisia Scale measures akathisia: a score of zero is none (good) maximum score is 12
Time Frame
8 weeks
Title
HbA1c
Description
Lab measure of glycated hemoglobin indicative of blood glucose over the last three months. At that time in the US measured as a percentage (of glucose attached to hemoglobin). No maximum or minimum but over 6.5% is generally considered indicative of diabetes.
Time Frame
8 weeks
Title
Insulin Level
Description
Measure of the amount of insulin in the blood, in uIU/ml. No minimum or maximum but fasting levels are usually below 25 uIU/ml. After a dose of glucose they may be 30 to 230 uIU/ml.
Time Frame
8 weeks
Title
Antipsychotic Medication Costs
Description
No data were collected because it turned out we had no way of measuring the costs. No subjects were analysed by costs
Time Frame
8 weeks

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
65 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Schizophrenia or schizoaffective Capacity to give consent Stable, on the same medication for a month but only partial response or with unacceptable side effects 18-65 years of age Exclusion Criteria: Repeated non-compliance Current depot medication Active medical conditions QTc >500msec Previous non-response Previous treatment with ziprasidone
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Nigel Bark, MD
Organizational Affiliation
Bronx Psychiatric Center
Official's Role
Principal Investigator
First Name & Middle Initial & Last Name & Degree
Jeffrey Grace, MD
Organizational Affiliation
Buffalo Psychiatric Center
Official's Role
Principal Investigator
First Name & Middle Initial & Last Name & Degree
Steven Schwarzkopf, MD
Organizational Affiliation
Rochester Psychiatric Center
Official's Role
Principal Investigator
Facility Information:
Facility Name
Bronx Psychiatric Center
City
Bronx
State/Province
New York
ZIP/Postal Code
10461
Country
United States
Facility Name
Buffalo Psychiatric Center
City
Buffalo
State/Province
New York
ZIP/Postal Code
14213
Country
United States

12. IPD Sharing Statement

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Efficacy and Tolerability of Switching to Ziprasidone From Other Antipsychotics

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