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NCT00061802 · ClinicalTrials.gov registry record · Phase 4

Efficacy and Safety of Two Atypical Antipsychotics vs. Placebo in Patients With an Acute Exacerbation of Either Schizophrenia or Schizoaffective Disorder

A Phase 4 study, sponsored by Johnson & Johnson Pharmaceutical Research & Development, L.L.C..

Completed
Registry status
Phase 4
Development phase
225
Enrollment target

NCT00061802: Completed Phase 4 study, sponsored by Johnson & Johnson Pharmaceutical Research & Development, L.L.C..

NCT00061802 is a Phase 4 study that has completed, run by Johnson & Johnson Pharmaceutical Research & Development, L.L.C.. The registered enrollment target is 225 participants, below the 518-participant average among 9,235 other Phase 4 trials with a reported enrollment target (57% lower). According to ClinicalTrials.gov, the official US trial registry.

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The verdict

NCT00061802, a Phase 4 study, has completed, sponsored by Johnson & Johnson Pharmaceutical Research & Development, L.L.C..

COMPLETED
Registry status
Phase 4
Development phase
225 participants
Enrollment target

Study Summary

A study to evaluate the efficacy and safety of two atypical antipsychotics vs. placebo in patients with an acute exacerbation of either schizophrenia or schizoaffective disorder

Interventions

  • DRUG risperidone, quetiapine

Trial Details

FieldValue
Enrollment Target 225 participants
Start Date 2003-06
Est. Completion 2004-02
Phase Phase 4

What the finished NCT00061802 record still lists

NCT00061802 is an interventional study that assigns participants to a tested intervention. The registered 225 participants enrollment target is mid-sized for trials with a published cap, below the 518-participant average among 9,235 other Phase 4 trials with a reported enrollment target (57% lower).

The record links to 0 conditions, and to 1 intervention - of which risperidone, quetiapine is the first listed.

NCT00061802 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT00061802 about?

NCT00061802 is a clinical study titled "Efficacy and Safety of Two Atypical Antipsychotics vs. Placebo in Patients With an Acute Exacerbation of Either Schizophrenia or Schizoaffective Disorder". A study to evaluate the efficacy and safety of two atypical antipsychotics vs. placebo in patients with an acute exacerbation of either schizophrenia or schizoaffective disorder

What is the current status of trial NCT00061802?

This trial is currently completed. It is a Phase 4 study. The enrollment target is 225 participants. The study started on 2003-06. Estimated completion is 2004-02.

What interventions are being tested in trial NCT00061802?

The interventions under investigation include: risperidone, quetiapine (DRUG).

Who is sponsoring clinical trial NCT00061802?

This trial is sponsored by Johnson & Johnson Pharmaceutical Research & Development, L.L.C., which has 102 total clinical trials registered on ClinicalTrials.gov.

How this trial's enrollment target compares

Where NCT00061802's enrollment target sits among peer trials

225 379th of 2000 higher than 1,622 of 2,000 other Phase 4 trials

participants (enrollment target), bucketed by value

Each bar is a band; taller bars hold more other Phase 4 trials. The dashed line + filled bar mark this entry. Hover or tap any bar for its full count and share, and where it sits relative to this entry.

Source ClinicalTrials.gov registry export · 2026-08-08

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Source: ClinicalTrials.gov NCT00061802, the US trial registry maintained by the National Library of Medicine. NCT00061802 (mid enrollment · none site footprint · completed) retrieved and formatted by PlainTrial, see methodology.