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Completed Phase 4 Interventional

Trial of Asthma Patient Education (TAPE)

ClinicalTrials.gov ID: NCT00148408

Public ClinicalTrials.gov record NCT00148408. 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 Sep 4, 2026, 1:15 AM EDT

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

Brief summary

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

The purpose of this research study is to investigate the way that educational approaches and presentation of a drug may affect the response to montelukast and placebo (an inactive medication) in subjects with asthma.

Study identification

NCT ID
NCT00148408
Recruitment status
Completed
Study type
Interventional
Phase
Phase 4
Enrollment
600 participants

Conditions and interventions

Conditions

Interventions

Drug · Behavioral

Eligibility (public fields only)

Age range
15 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
Nov 30, 2003
Primary completion
Nov 30, 2005
Completion
Nov 30, 2005
Last update posted
Apr 29, 2010

2003 – 2005

United States locations

U.S. sites
20
U.S. states
16
U.S. cities
20
Facility City State ZIP Site status
University of Alabama at Birmingham Birmingham Alabama 35233
University of California at San Diego San Diego California 92103
National Jewish Hospital Denver Colorado 80206
Nemour's Childrens Center Jacksonville Florida 32207
University of Miami (and University of South Florida in Tampa) Miami Florida 33136
Emory University Atlanta Georgia 30322
Illinois Consortium (Northwestern, Univ. of Chicago, Univ. of Illinois) Chicago Illinois 60611
Indiana University Indianapolis Indiana 46202
Louisiana State University New Orleans Louisiana 70112
University of Minnesota Minneapolis Minnesota 55455
University of Missouri at Kansas City Kansas City Missouri 64108
Washington University St Louis Missouri 63110
Long Island Jewish Hospital (and North Shore Hospital) New Hyde Park New York 11040
New York Consortium (New York Univ. and Columbia Univ.) New York New York 10016
New York Medical College Valhalla New York 10595
Duke University School of Medicine Durham North Carolina 27710
Ohio State University Columbus Ohio 43210
Thomas Jefferson Hospital Philadelphia Pennsylvania 19107
Baylor College of Medicine Houston Texas 77030
Northern New England Consortium (Univ. of Vermont and other locations) Burlington Vermont 05405

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 NCT00148408, 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 Apr 29, 2010 · Synced Sep 4, 2026

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Open the official record

The complete protocol, eligibility criteria, and contact information for NCT00148408 live on ClinicalTrials.gov.

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