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Clinical Trials/NL-OMON34837
NL-OMON34837
Completed
Phase 4

Evaluation of Growth, Sexual Maturation, and Prolactin-Related Adverse Events in the Pediatric Population Exposed to Atypical Antipsychotic Drugs - Growth, Sexual Mat., Prolactin-Rel. AEs in Children Exp. to Antipsychotics

Janssen-Cilag0 sites40 target enrollmentTBD

Overview

Phase
Phase 4
Intervention
Not specified
Conditions
Not specified
Sponsor
Janssen-Cilag
Enrollment
40
Status
Completed
Last Updated
last year

Overview

Brief Summary

No summary available.

Registry
who.int
Start Date
TBD
End Date
TBD
Last Updated
last year
Study Type
Observational invasive

Investigators

Eligibility Criteria

Inclusion Criteria

  • Subjects will only be included in the study sample if they meet all of the following criteria:
  • 1\. Boys and girls 8 to 16 years of age;
  • 2\. One or both parents (according to local regulations) or a guardian must have signed an informed consent document indicating that they understand the purpose of and procedures required for the study and are willing to participate in the study. If appropriate according to local regulations, the subject must also assent;
  • 3\. Treated for schizophrenia, bipolar mania, autistic disorder, or conduct and other disruptive behavior disorders;
  • 4\. Had at least 6 months of exposure for an atypical antipsychotic drug within 24 months before the study visit; subjects may or may not be taking the atypical antipsychotics at the time of actual enrollment; eligible subjects can have exposure to multiple atypical antipsychotics. However, they cannot concomitantly be exposed to more than one atypical antipsychotic for a period of \>30 days (to allow for cross\-taper) (Section 12\.2\.);
  • 5\. Had medical records or automated data available for at least 1 year prior to the start of exposure;
  • 6\. Height and weight were recorded at least once within one year before the start of exposure, and if available at any time points after the start of exposure in the medical records or electronic databases (not mandatory).

Exclusion Criteria

  • Subjects will be excluded from this study sample if they:
  • 1\. Have at least 1 medical record, at any time before the start of exposure, consistent with malignancy (other than non\-melanoma skin cancer), pregnancy, or a developmental delay or abnormality associated with growth or sexual maturation delays not related to the specified indications (Section 12\.3\.);
  • 2\. Had exposure to prolactin elevating medications (Section 12\.1\.2\.) other than atypical antipsychotics and selective serotonin reuptake inhibitors (SSRIs);
  • 3\. Had exposure to Paliperidone;
  • 4\. Cannot comply with study procedures.

Outcomes

Primary Outcomes

Not specified

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