Olanzapine Versus An Active Comparator in the Treatment of Schizophrenia

NCT ID: NCT00036088

Last Updated: 2006-07-19

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

Get a concise snapshot of the trial, including recruitment status, study phase, enrollment targets, and key timeline milestones.

Recruitment Status

COMPLETED

Clinical Phase

PHASE4

Total Enrollment

530 participants

Study Classification

INTERVENTIONAL

Study Start Date

2001-08-31

Study Completion Date

2002-07-31

Brief Summary

Review the sponsor-provided synopsis that highlights what the study is about and why it is being conducted.

The purpose of this study is to determine how Olanzapine compares to an active comparator in the treatment of schizophrenia

Detailed Description

Dive into the extended narrative that explains the scientific background, objectives, and procedures in greater depth.

Conditions

See the medical conditions and disease areas that this research is targeting or investigating.

Schizophrenia

Study Design

Understand how the trial is structured, including allocation methods, masking strategies, primary purpose, and other design elements.

Allocation Method

RANDOMIZED

Intervention Model

PARALLEL

Primary Study Purpose

TREATMENT

Blinding Strategy

DOUBLE

Interventions

Learn about the drugs, procedures, or behavioral strategies being tested and how they are applied within this trial.

Olanzapine

Intervention Type DRUG

Eligibility Criteria

Check the participation requirements, including inclusion and exclusion rules, age limits, and whether healthy volunteers are accepted.

Inclusion Criteria

1. You must be between the ages of 18 and 75. If you have reached your 76th birthday, you will not be able to participate
2. You must have been diagnosed with schizophrenia
3. You must be able to visit the doctor's office as scheduled for the next 7 months

Exclusion:

1. You have a serious medical illness, such as heart, liver, or kidney disease (Note: If you are uncertain about a particular condition, discuss it with your doctor.)
2. You are either pregnant or breastfeeding
Minimum Eligible Age

18 Years

Maximum Eligible Age

75 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

Yes

Sponsors

Meet the organizations funding or collaborating on the study and learn about their roles.

Eli Lilly and Company

INDUSTRY

Sponsor Role lead

Locations

Explore where the study is taking place and check the recruitment status at each participating site.

El Centro, California, United States

Site Status

Glendale, California, United States

Site Status

Sherman Oaks, California, United States

Site Status

Middleton, Connecticut, United States

Site Status

Norwich, Connecticut, United States

Site Status

Melbourne, Florida, United States

Site Status

Miami, Florida, United States

Site Status

Atlanta, Georgia, United States

Site Status

Chicago, Illinois, United States

Site Status

Hoffman Estates, Illinois, United States

Site Status

Lafayette, Indiana, United States

Site Status

Rockville, Maryland, United States

Site Status

Newton, Massachusetts, United States

Site Status

Saint Charles, Missouri, United States

Site Status

New York, New York, United States

Site Status

Olean, New York, United States

Site Status

Staten Island, New York, United States

Site Status

Cincinnati, Ohio, United States

Site Status

Portland, Oregon, United States

Site Status

Philadelphia, Pennsylvania, United States

Site Status

Austin, Texas, United States

Site Status

El Paso, Texas, United States

Site Status

Houston, Texas, United States

Site Status

Terrell, Texas, United States

Site Status

Richmond, Virginia, United States

Site Status

La Plata, Buenos Aires, Argentina

Site Status

Godoy Cruz, Mendoza Province, Argentina

Site Status

Buenos Aires, , Argentina

Site Status

Ciudad de Buenos Air, , Argentina

Site Status

Graz, , Austria

Site Status

Innsbruck, , Austria

Site Status

Linz, , Austria

Site Status

Wein, , Austria

Site Status

Wels, , Austria

Site Status

Salvador, Estado de Bahia, Brazil

Site Status

Aparecida de Goiânia, Goiás, Brazil

Site Status

Pelotas, Rio Grande do Sul, Brazil

Site Status

Sau Paulo, Sau Paulo, Brazil

Site Status

Rio de Janeiro, , Brazil

Site Status

Essen, , Germany

Site Status

Hamburg, , Germany

Site Status

Tübingen, , Germany

Site Status

Dublin, , Ireland

Site Status

Mexico City, , Mexico

Site Status

Lima, , Peru

Site Status

Cidra, , Puerto Rico

Site Status

Ponce, , Puerto Rico

Site Status

Rio Piedras, , Puerto Rico

Site Status

San Juan, , Puerto Rico

Site Status

Barcelona, Barcelona, Spain

Site Status

San Boi de Llobregat, Barcelona, Spain

Site Status

Elizondo, Navarre, Spain

Site Status

Pamplona, Navarre, Spain

Site Status

Langreo, Principality of Asturias, Spain

Site Status

Camberwell, London, United Kingdom

Site Status

London, London, United Kingdom

Site Status

Kings Lynn, Norfolk, United Kingdom

Site Status

Paisley, Scotland, United Kingdom

Site Status

Guildford, Surrey, United Kingdom

Site Status

Caracas, , Venezuela

Site Status

Countries

Review the countries where the study has at least one active or historical site.

United States Argentina Austria Brazil Germany Ireland Mexico Peru Puerto Rico Spain United Kingdom Venezuela

References

Explore related publications, articles, or registry entries linked to this study.

Liu-Seifert H, Ascher-Svanum H, Osuntokun O, Jen KY, Gomez JC. Change in level of productivity in the treatment of schizophrenia with olanzapine or other antipsychotics. BMC Psychiatry. 2011 May 17;11:87. doi: 10.1186/1471-244X-11-87.

Reference Type DERIVED
PMID: 21586165 (View on PubMed)

Other Identifiers

Review additional registry numbers or institutional identifiers associated with this trial.

F1D-MC-HGHJ

Identifier Type: -

Identifier Source: secondary_id

2347

Identifier Type: -

Identifier Source: org_study_id