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Completed Phase 4 Interventional

A Study of Risperidone Monotherapy in Bipolar Anxiety

ClinicalTrials.gov ID: NCT00167479

Public ClinicalTrials.gov record NCT00167479. Field values are reproduced from the official study page; the official ClinicalTrials.gov record remains the source of truth for eligibility, enrollment, and contact information.

ClinicalTrials.gov public records Last synced May 5, 2026, 4:32 AM EDT

Data is sourced from official ClinicalTrials.gov public API records. Always review the official ClinicalTrials.gov record for the latest information.

Official title

A Randomized, Double-Blind, Placebo-Controlled Study of Risperidone Monotherapy in Ambulatory Bipolar Disorder With Current at Least Moderately Severe Anxiety and Lifetime Panic Disorder or Generalized Anxiety Disorder

Study identification

NCT ID
NCT00167479
Recruitment status
Completed
Study type
Interventional
Phase
Phase 4
Lead sponsor
University of South Florida
Other
Enrollment
60 participants

Conditions and interventions

Interventions

  • risperidone (Risperdal) Drug

Drug

Eligibility (public fields only)

Age range
18 Years and older
Sex
All
Healthy volunteers
Healthy volunteers not accepted

This page does not interpret eligibility. Detailed inclusion and exclusion criteria are on the official ClinicalTrials.gov record.

Study timeline

Start date
Aug 31, 2003
Primary completion
Not listed
Completion
Aug 31, 2006
Last update posted
Sep 10, 2006

2003 – 2006

United States locations

U.S. sites
3
U.S. states
3
U.S. cities
3
Facility City State ZIP Site status
University of South Florida Psychiatry Center Tampa Florida 33613-4788
University of Cincinatti Cincinnati Ohio
University of Texas Southwestern Medical Center Dallas Texas

Site contact phone numbers, emails, and investigator names are intentionally not displayed here. Open the official ClinicalTrials.gov record for site contact information.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT00167479, including study identification, conditions, interventions, eligibility (age, sex, healthy volunteer), timeline, and U.S. site list.
What this page does not do
No medical advice, eligibility judgments, treatment recommendations, study quality scoring, or AI-generated medical summaries. No site contact phone numbers, emails, or investigator names.
Where the data comes from
Sourced from the official ClinicalTrials.gov public API. The official record is the source of truth.
Last refresh
Last update posted Sep 10, 2006 · Synced May 5, 2026

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Open the official record

The complete protocol, eligibility criteria, and contact information for NCT00167479 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →