Study of Safety of Foradil in Patients With Persistent Asthma
Public ClinicalTrials.gov record NCT01845025. 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.
Data is sourced from official ClinicalTrials.gov public API records. Always review the official ClinicalTrials.gov record for the latest information.
Official title
A 26 Week, Randomized, Active-controlled Safety Study of Double-blind Formoterol Fumarate in Free Combination With an Inhaled Corticosteroid Versus an Inhaled Corticosteroid in Adolescent and Adult Patients With Persistent Asthma.
Brief summary
Reproduced verbatim from the official ClinicalTrials.gov record. Not medical advice.
The purpose of this study was to assess whether the risk of serious asthma-related events (asthma-related hospitalizations, asthma related intubations, and asthma related deaths) in adolescents and adults (12 years of age and older) taking inhaled formoterol fumarate/fluticasone propionate combination was the same as those taking inhaled fluticasone propionate alone.
Study identification
- NCT ID
- NCT01845025
- Recruitment status
- Terminated
- Study type
- Interventional
- Phase
- Phase 4
- Enrollment
- 827 participants
Conditions and interventions
Conditions
Interventions
- Formoterol 12 mcg Drug
- Fluticasone propionate 100 mcg Drug
- Fluticasone propionate 250 mcg Drug
- Fluticasone propionate 500 mcg Drug
- Placebo Drug
Drug
Eligibility (public fields only)
- Age range
- 12 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
- Apr 30, 2013
- Primary completion
- Apr 30, 2016
- Completion
- Apr 30, 2016
- Last update posted
- Mar 20, 2017
2013 – 2016
United States locations
- U.S. sites
- 27
- U.S. states
- 19
- U.S. cities
- 24
| Facility | City | State | ZIP | Site status |
|---|---|---|---|---|
| Novartis Investigative Site | Avondale | Arizona | 85323 | — |
| Novartis Investigative Site | North Hollywood | California | 91606 | — |
| Novartis Investigative Site | Bradenton | Florida | 34209 | — |
| Novartis Investigative Site | Miami | Florida | 33126 | — |
| Novartis Investigative Site | Miami | Florida | 33134 | — |
| Novartis Investigative Site | Conyers | Georgia | 30012 | — |
| Novartis Investigative Site | Stone Mountain | Georgia | 30083 | — |
| Novartis Investigative Site | Louisville | Kentucky | 40214 | — |
| Novartis Investigative Site | Louisville | Kentucky | 40220 | — |
| Novartis Investigative Site | Covington | Louisiana | 70433 | — |
| Novartis Investigative Site | Baltimore | Maryland | 21287 | — |
| Novartis Investigative Site | Gaithersburg | Maryland | 20878 | — |
| Novartis Investigative Site | Picayune | Mississippi | 39466 | — |
| Novartis Investigative Site | St Louis | Missouri | 63117 | — |
| Novartis Investigative Site | St Louis | Missouri | 63128 | — |
| Novartis Investigative Site | North Massapequa | New York | 11758 | — |
| Novartis Investigative Site | Elizabeth City | North Carolina | 27909 | — |
| Novartis Investigative Site | Winston-Salem | North Carolina | 27103 | — |
| Novartis Investigative Site | Cleveland | Ohio | 44106-5000 | — |
| Novartis Investigative Site | Oaks | Pennsylvania | 19456 | — |
| Novartis Investigative Site | East Greenwich | Rhode Island | 02818 | — |
| Novartis Investigative Site | Mt. Pleasant | South Carolina | 29464 | — |
| Novartis Investigative Site | Memphis | Tennessee | 38118 | — |
| Novartis Investigative Site | Dallas | Texas | 75235 | — |
| Novartis Investigative Site | St. George | Utah | 84790 | — |
| Novartis Investigative Site | Mequon | Wisconsin | 53092 | — |
| Novartis Investigative Site | Milwaukee | Wisconsin | 53172 | — |
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 NCT01845025, 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 Mar 20, 2017 · Synced Sep 3, 2026
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Open the official record
The complete protocol, eligibility criteria, and contact information for NCT01845025 live on ClinicalTrials.gov.