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Completed Phase 4 Interventional

Costs & Outcomes of Hospitalization/Treatment With Levalbuterol & Albuterol in Asthma or Chronic Obstructive Pulmonary Disease (COPD) Subjects

ClinicalTrials.gov ID: NCT00667797

Public ClinicalTrials.gov record NCT00667797. 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 Oct 22, 2026, 6:01 PM EDT

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

Official title

Pharmacoeconomic Outcomes of Levalbuterol and Racemic Albuterol in Inpatients Requiring Nebulization (POLARIS)

Brief summary

Reproduced verbatim from the official ClinicalTrials.gov record. Not medical advice.

An analysis of the costs and outcomes associated with hospitalization and treatment of Levalbuterol versus Racemic Albuterol in subjects with Asthma and COPD.

Study identification

NCT ID
NCT00667797
Recruitment status
Completed
Study type
Interventional
Phase
Phase 4
Lead sponsor
Sumitomo Pharma America, Inc.
Industry
Enrollment
486 participants

Conditions and interventions

Conditions

Interventions

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
Mar 2003 (Type not available)
Primary completion
May 2005 (Actual)
Completion
May 2005 (Actual)
Last update posted
Feb 22, 2012

2003 – 2005

United States locations

U.S. sites
18
U.S. states
14
U.S. cities
18
Facility City State ZIP Site status
Not listed Birmingham Alabama — —
Not listed Chula Vista California — —
Not listed Oakland California — —
Not listed Wheat Ridge Colorado — —
Not listed Waterbury Connecticut — —
Not listed Washington D.C. District of Columbia — —
Not listed Brandon Florida — —
Not listed Des Moines Iowa — —
Not listed Johnson City New Jersey — —
Not listed Great Neck New York — —
Not listed Syracuse New York — —
Not listed Chapel Hill North Carolina — —
Not listed Winston-Salem North Carolina — —
Not listed Portland Oregon — —
Not listed Pittsburgh Pennsylvania — —
Not listed Houston Texas — —
Not listed San Antonio Texas — —
Not listed Morgantown West Virginia — —

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 NCT00667797, 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 Feb 22, 2012 · Synced Oct 22, 2026

Related: full search, browse by condition, browse by drug or therapy, browse by sponsor, browse by U.S. city.

Open the official record

The complete public registry record, listed eligibility criteria, and available contact information for NCT00667797 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →