NCT Number: NCT00199940
Safety And Efficacy Study Of Ziprasidone In Pediatric Psychotic Illness
The purpose of this research is to determine if Ziprasidone is safe and effective for use in children and adolescents with a psychotic illness, and to determine of Ziprasidone treatment leads to weight changes in children.
Looking for future studies?
Notify MeKey information
Conditions
Age range
7 year–17 year
Sex eligibility
All sexes
Study type
Interventional
Phase
Phase 4
About this study
Ziprasidone is a recently FDA approved antipsychotic, and it holds promise in the treatment of pediatric psychosis due to its low liability for weight gain and other side effects. This is important because early intervention in persons with a psychotic illness is important for their long-term treatment and outcome. Unfortunately, pediatric samples are often more sensitive to the side effects of psychotropic medications. Because psychotropic medications are often used by clinicians long before they are studied in pediatric populations, it is important to further study these agents.
Twenty subjects with the diagnosis of a psychotic disorder, according to DSM-IV criteria, will be recruited for the study. If subjects have completed baseline evaluations, labs, EKG, and rating scales and are still eligible to participate, subjects will start on 20mg of Ziprasidone at night. The second week this will increase to 20 mg twice a day. At visits that occur at 2,4,6,and 8 weeks, the subject's dose of medication can be increased in 20mg per day increments. This allows for a maximum possible dose of 100mg. Dosage may be decreased at any time secondary to side effects.
The potential benefits are that new information will be added to the field of pediatric psychiatry and the possibility that the medication may result in improved symptoms of psychosis. The potential benefits of this study outweigh the possible risks.
Who can participate
Healthy volunteers accepted: No
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
- Diagnosis of Schizophrenia, Schizophreniform DO, Schizoaffective DO or Psychotic Disorder NOS
- Male/female, ages 7.0-17 years old
- Normal intelligence, ability to provide assent and consent
- Not currently receiving adequate treatment
Exclusion criteria
- Known hypersensitivity to ziprasidone (past failed trial)
- History of QTc prolongation
- Recent myocardial infarction
- Uncompensated heart failure
- Currently treated with other QTc prolonging medications
- Unstable medical illness
- If on diuretics, monitor regularly for hypokalemia
Treatment and study plan
Primary outcomes
-
Positive and Negative Symptom Scale (PANSS), score symptoms from baseline through end of study Week 8.
Secondary outcomes
-
Kiddie Schedule for Affective Disorders and Schizophrenia (K-SADS), assess at baseline only.
-
Child Depression Rating Scale (CDRS), rate from baseline to Week 8.
-
Simpson-Angus Rating Scale (SARS), rate from baseline to Week 8.
-
Abnormal Involuntary Movement Scale (AIMS), rate at baseline, Weeks 2,4,6,8.
-
Barnes Akathesia Scale (BAS), rate from baseline through Week 8.
-
Side-Effect For Children & Adolescents (SEFCA), rate from baseline through Week 8.
Sponsors and collaborators
Lead sponsor
Medical College of Wisconsin
Other
Registry information
Official study title
A Pilot Open Trial Of Ziprasidone, Early In The Course Of Pediatric Psychotic Illness
Important dates
- Study start
- 2003
- Study completion
- 2007
- First posted
- Sep 20, 2005
- Registry last updated
- Mar 12, 2008
OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.
View the official ClinicalTrials.gov record (opens in a new tab)This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.
Related clinical trials
Published trials that share one or more normalized conditions with this study.
Early Psychosis Intervention - Spreading Evidence-based Treatment
NCT03919760
Affective Disorders, Psychotic, Behavior
Greater Sudbury, Ontario, Canada
View Trial DetailsED to EPI: Using SMS to Improve the Transition From the Emergency Department to Early Psychosis Intervention
NCT04298450
Affective Disorders, Psychotic, Bipolar Disorder
Toronto, Ontario, Canada
View Trial DetailsCannabis, Schizophrenia and Reward: Self-Medication and Agonist Treatment?
NCT01964404
Cannabis Use Disorder, Chemically-Induced Disorders
Lebanon, New Hampshire, United States
View Trial DetailsRemote State Representation in Early Psychosis
NCT05538832
Affective Disorders, Psychotic, Mental Disorders
Minneapolis, Minnesota, United States
View Trial Details