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A Study Evaluating the Efficacy and Impact on Health-related Quality of Life of Levocetirizine in Adults With Seasonal Allergic Rhinitis
NCT00621959 · View on ClinicalTrials.gov ↗
Study Summary
The study objective is to investigate the efficacy of levocetirizine in reducing symptoms associated with seasonal allergic rhinitis and in improving rhinitis-related Quality of Life
Conditions Studied
Interventions
- DRUG placebo
- DRUG levocetirizine dihydrochloride
Study Locations (20)
California
- — Huntington Beach
- — Long Beach
- — Los Angeles
- — Mission Viejo
Texas
- — Austin
- — Dallas
- — El Paso
- — Fort Worth
Georgia
- — Albany
- — Lilburn
- — Savannah
Arkansas
- — Hot Springs
- — Little Rock
Arizona
- — Scottsdale
Kentucky
- — Owensboro
Louisiana
- — Metairie
North Carolina
- — Winston-Salem
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 596 participants |
| Start Date | 2008-03 |
| Est. Completion | 2008-06 |
| Phase | Phase 4 |
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Full Details on ClinicalTrials.gov ↗What the Registry Record Tells You About NCT00621959
The ClinicalTrials.gov registry entry for NCT00621959 describes a study currently listed as completed. It is categorized as Phase 4, 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 596 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is UCB Pharma, which has 20 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 2 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: NCT00621959 reports 20 study locations spanning 11 distinct geographic areas — top geographies include California, Texas, Georgia. 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 NCT00621959 about?
NCT00621959 is a clinical study titled "A Study Evaluating the Efficacy and Impact on Health-related Quality of Life of Levocetirizine in Adults With Seasonal Allergic Rhinitis". The study objective is to investigate the efficacy of levocetirizine in reducing symptoms associated with seasonal allergic rhinitis and in improving rhinitis-related Quality of Life
What is the current status of trial NCT00621959?
This trial is currently completed. It is a Phase 4 study. The enrollment target is 596 participants. The study started on 2008-03. Estimated completion is 2008-06.
What conditions does trial NCT00621959 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 NCT00621959?
The interventions under investigation include: placebo (DRUG), levocetirizine dihydrochloride (DRUG). Each intervention is being evaluated for safety and efficacy as part of this clinical study.
Who is sponsoring clinical trial NCT00621959?
This trial is sponsored by UCB Pharma, which has 20 total clinical trials registered on ClinicalTrials.gov. The sponsor is responsible for the study's design, funding, and regulatory compliance.
Where is trial NCT00621959 being conducted?
This trial has 20 study locations across Arizona, Arkansas, California, Georgia, Kentucky. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.
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