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Completed

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.

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Key information

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

Ziprasidone

Drug

Primary outcomes

  1. Positive and Negative Symptom Scale (PANSS), score symptoms from baseline through end of study Week 8.

Secondary outcomes

  1. Kiddie Schedule for Affective Disorders and Schizophrenia (K-SADS), assess at baseline only.

  2. Child Depression Rating Scale (CDRS), rate from baseline to Week 8.

  3. Simpson-Angus Rating Scale (SARS), rate from baseline to Week 8.

  4. Abnormal Involuntary Movement Scale (AIMS), rate at baseline, Weeks 2,4,6,8.

  5. Barnes Akathesia Scale (BAS), rate from baseline through Week 8.

  6. 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.

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