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COMPLETEDPhase 4NCT00979615

Safety and Efficacy of Olopatadine 0.6% and Azelastine 137 Mcg in Vasomotor Rhinitis

The purpose of this study is to examine safety and efficacy of Patanase and Astelin in treating the symptoms of non-allergic vasomotor rhinitis (VMR).

Lead sponsor: Alcon Research•1 U.S. locations•View source on ClinicalTrials.gov

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Sponsors

Lead Sponsor

Alcon Research

Age

12 - No limit years

Sex

ALL

Healthy Volunteers

No

Inclusion Criteria

•Diagnosis of VMR with at least 2 years of chronic non-allergic rhinitis
•Negative skin tests to a panel of allergens and positive histamine test within last 2 years
•History of symptoms related to defined VMR triggers

Exclusion Criteria

•Nasal disorder, surgery, or concurrent disease that could interfere with evaluation of study medications
•Bacterial or viral infection within 14 days of first visit. Diagnosis of acute sinusitis within 30 days of first visit
•Chronic use of drugs that can cause rhinitis

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Data from ClinicalTrials.govLast updated on ClinicalTrials.gov: May 10, 2011Terms

Trial snapshot

StatusCOMPLETED

PhasePHASE4

Enrollment129

Start dateSep 2009

Last updatedMay 10, 2011

Condition

Vasomotor Rhinitis

Locations shown

Contact Alcon Call Center For Trial Locations

Fort Worth, Texas

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Data Source & Attribution

This clinical trial information is sourced from ClinicalTrials.gov, a service of the U.S. National Institutes of Health.

ClinicalTrials.gov last update: May 10, 2011Data synced to Clareo: June 28, 2026

Modifications: This data has been reformatted for display purposes. Eligibility criteria have been parsed into inclusion/exclusion sections. Location data has been geocoded to enable distance-based search. For the authoritative and most current information, please visit ClinicalTrials.gov.

Neither the United States Government nor Clareo Health make any warranties regarding the data. Check ClinicalTrials.gov frequently for updates.

View ClinicalTrials.gov Terms and Conditions