Bipolar Disorder, Depressive Disorder, Major, Psychosis, Schizoaffective Disorder, Schizophreniform Disorder
Conditions
Keywords
psychosis NOS, MDD w/ psychotic features, bipolar disorder w. psychotic features
Brief summary
This open-label study will assess the medication Geodon® (Ziprasidone) in pediatric patients, aged 13-17, diagnosed with psychotic disorder. Eligible adolescents will receive Geodon® for 7 weeks and stay at the NYSPI Children's Day Unit (CDU) during the day. If clinically appropriate, they may also stay at the New York State Psychiatric Institute (NYSPI) Schizophrenia Research Unit (SRU) inpatient facility.
Detailed description
This study is an open-label assessment of the feasibility of treating adolescents with psychotic disorders (schizophreniform disorder, schizoaffective disorder, psychosis not otherwise specified \[NOS\], major depressive disorder with psychotic features, and bipolar disorder with psychotic features) in an inpatient and day hospital setting with ziprasidone (Geodon). Ziprasidone is a second-generation antipsychotic (SGA) that is FDA-approved for the treatment of schizophrenia and for the treatment of the manic phase of bipolar disorder in adults. It is also used clinically in the treatment of psychotic disorders in children, adolescents and adults. This protocol will help to elucidate the feasibility of studying the treatment of psychotic disorders with ziprasidone in adolescents 13-17 years and help facilitate the further study of the treatment of psychosis with novel agents that have a favorable side effect and weight gain profile. The duration of the study can be up to 7 weeks. Depending on the level of symptom severity patients will be managed on either the Schizophrenia Research Unit (SRU) (GAS\<35, CGI-S\>5), or the Children's Day Unit (CDU) of the NYSPI. The seven weeks would encompass a 3 day period at the beginning of the study including time for screening and reviewing lab results. Over a period of one to two weeks patients will be titrated up to 120 mg/day (80 mg for patients under 45kg), and, if necessary, cross tapered off of another SGA that had not been working successfully. Subjects who do not respond to the medication after 1 week at the target dose will be discontinued from the study.
Interventions
DRUGZiprasidone
subjects will use ziprasidone
Sponsors
Pfizer
New York State Psychiatric Institute
Study design
Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
TREATMENT
Masking
NONE
Eligibility
Sex/Gender
ALL
Age
13 Years to 17 Years
Healthy volunteers
No
Inclusion criteria
1. Children who meet DSM-IV criteria for the following psychotic disorders: schizophreniform disorder, schizoaffective disorder, psychosis NOS, major depressive disorder with psychotic features, and bipolar disorder with psychotic features. 2. Children with an IQ of at least 70. 3. Children who are in good physical health. 4. The parent/guardian of the child must be willing to attend all study visits.
Exclusion criteria
1. Children who are currently receiving an effective treatment without detrimental side effects. 2. Children who are allergic to Geodon®. 3. Children who have previously failed to respond to an adequate trial of Geodon®. 4. Females who are pregnant or breast-feeding.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Weight Gain and Other Side Effects | couple of months |
Countries
United States
Participant flow
Recruitment details
P.I. has left the institution and NYSPI has no access to the data. Results will not be analyzed or presented.
Participants by arm
| Arm | Count |
|---|---|
| Ziprasidone Ziprasidone: subjects will use ziprasidone | 0 |
| Total | 0 |
Baseline characteristics
| Characteristic | — |
|---|---|
| Region of Enrollment United States | — participants |
Adverse events
| Event type | EG000 affected / at risk |
|---|---|
| deaths Total, all-cause mortality | — / — |
| other Total, other adverse events | 0 / 0 |
| serious Total, serious adverse events | 0 / 0 |
Outcome results
Primary
Weight Gain and Other Side Effects
Time frame: couple of months
Population: P.I. has left the institution and NYSPI has no access to the data. Results will not be analyzed or presented.