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A Study Evaluating the Safety and Effectiveness of a Nasal Spray to Treat Seasonal Allergies
NCT00740792 · View on ClinicalTrials.gov ↗
Study Summary
The purpose of this study is to determine if two allergy medications (formulated azelastine and fluticasone product) are more effective than placebo or either medication alone (azelastine or fluticasone)
Conditions Studied
Interventions
- DRUG placebo
- DRUG azelastine HCl/fluticasone propionate
- DRUG azelastine Hcl
- DRUG fluticasone propionate
Study Locations (20)
California
- Clinical Research Center — Encinitas
- AABI Associates Medical Group — Fountain Valley
- William Ebbling, MD Inc — Fresno
- Allergy & Asthma Care Center of So. Cal — Long Beach
- Allergy Research Foundation — Los Angeles
- Southern California Research — Mission Viejo
- Allergy Associates Medical Group Inc — San Diego
- Bensch Research Associates — Stockton
Georgia
- Clinical Research Atlanta — Atlanta
- Atlanta Allergy and Asthma Clinic — Stockbridge
- Clinical Research Atlanta — Stockbridge
Colorado
- Storms Clinical Research Institute — Colorado Springs
- Colorado Allergy and Asthma Centers — Denver
Minnesota
- Clinical Reseacrh Institute — Minneapolis
- Clinical Research Institute — Plymouth
Arizona
- Allergy, Asthma and Immunology Associates — Scottsdale
Illinois
- Sneeze, Wheeze and Itch Associates — Normal
Kansas
- Kansas City Allergy and Asthma — Overland Park
Massachusetts
- Northeast Medical Research Associates — North Dartmouth
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 776 participants |
| Start Date | 2008-08 |
| Est. Completion | 2008-11 |
| Phase | Phase 3 |
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Full Details on ClinicalTrials.gov ↗What the Registry Record Tells You About NCT00740792
The ClinicalTrials.gov registry entry for NCT00740792 describes a study currently listed as completed. It is categorized as Phase 3, which is the standard way researchers label where a study sits along the investigational pathway from early safety work through later efficacy and post-marketing evaluation. The registered enrollment target is 776 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is Meda Pharmaceuticals, which has 3 total studies on file at ClinicalTrials.gov, and sponsors are the parties responsible for study design, oversight, and regulatory filings.
The record links to 1 condition, with Seasonal Allergic Rhinitis appearing as the primary indexed condition, and to 4 interventions — of which placebo is the first listed. Interventions can include drugs, devices, procedures, behavioral programs, or observational arms, and each is tracked as a separate registry field so that downstream queries can filter accurately. When a trial lists multiple interventions, it usually reflects a multi-arm design or a comparison protocol rather than a single treatment being tested in isolation. The brief summary published in the registry is the clearest source of protocol intent and should be read before drawing conclusions from any sidebar tags.
Geographic footprint matters for practical reasons: NCT00740792 reports 20 study locations spanning 9 distinct geographic areas — top geographies include California, Georgia, Colorado. A larger site network tends to correlate with broader recruitment capacity, but it does not imply anything about study quality, and site-level enrollment status can diverge from the overall registry status shown above. Every data point on this page comes from the public ClinicalTrials.gov dataset and is reproduced here for reference only; it is not a medical recommendation, an endorsement of the sponsor, or an invitation to enroll. Verify current status, eligibility criteria, and contact details directly at ClinicalTrials.gov, and discuss any participation decision with your own healthcare provider.
Frequently Asked Questions
What is clinical trial NCT00740792 about?
NCT00740792 is a clinical study titled "A Study Evaluating the Safety and Effectiveness of a Nasal Spray to Treat Seasonal Allergies". The purpose of this study is to determine if two allergy medications (formulated azelastine and fluticasone product) are more effective than placebo or either medication alone (azelastine or fluticasone)
What is the current status of trial NCT00740792?
This trial is currently completed. It is a Phase 3 study. The enrollment target is 776 participants. The study started on 2008-08. Estimated completion is 2008-11.
What conditions does trial NCT00740792 study?
This clinical trial studies the following conditions: Seasonal Allergic Rhinitis. These conditions were identified from the trial registry and reflect the primary focus areas of the research.
What interventions are being tested in trial NCT00740792?
The interventions under investigation include: placebo (DRUG), azelastine HCl/fluticasone propionate (DRUG), azelastine Hcl (DRUG), fluticasone propionate (DRUG). Each intervention is being evaluated for safety and efficacy as part of this clinical study.
Who is sponsoring clinical trial NCT00740792?
This trial is sponsored by Meda Pharmaceuticals, which has 3 total clinical trials registered on ClinicalTrials.gov. The sponsor is responsible for the study's design, funding, and regulatory compliance.
Where is trial NCT00740792 being conducted?
This trial has 20 study locations across Arizona, California, Colorado, Georgia, Illinois. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.
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