An Observational Study to Assess Treatment & Outcomes Data in Patients Receiving Long-Acting Injectable Risperidone

NCT00774085 · Status: COMPLETED · Type: OBSERVATIONAL · Enrollment: 408

Last updated 2012-04-27

No results posted yet for this study

Summary

The purpose of this study is to assess treatment and outcomes data in patients receiving treatment with long-acting injectable risperidone.

Conditions

Interventions

OTHER

No intervention was given

Participants included patients treated with long-acting injectable risperidone (Risperdal Consta) in daily practice according to local label by the physicians

Sponsors & Collaborators

  • Janssen Cilag N.V./S.A.

    lead INDUSTRY

Principal Investigators

  • Janssen-Cilag N.V./S.A., Belgium Clinical Trial · Janssen Cilag N.V./S.A.

Eligibility

Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2004-11-30
Primary Completion
2007-12-31
Completion
2007-12-31

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Entities

Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT00774085 on ClinicalTrials.gov