Safety Study of Olopatadine Nasal Spray
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The safety and scientific validity of this study is the responsibility of the study sponsor and investigators. Listing a study does not mean it has been evaluated by the U.S. Federal Government. Read our disclaimer for details. |
ClinicalTrials.gov Identifier: NCT00578331 |
Recruitment Status :
Completed
First Posted : December 21, 2007
Results First Posted : February 3, 2010
Last Update Posted : October 31, 2017
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Condition or disease | Intervention/treatment | Phase |
---|---|---|
Perennial Allergic Rhinitis | Drug: Olopatadine 0.6% nasal spray Drug: Placebo Nasal Spray | Phase 3 |
Study Type : | Interventional (Clinical Trial) |
Actual Enrollment : | 890 participants |
Allocation: | Randomized |
Intervention Model: | Parallel Assignment |
Masking: | Quadruple (Participant, Care Provider, Investigator, Outcomes Assessor) |
Primary Purpose: | Treatment |
Official Title: | Safety Study of Olopatadine Nasal Spray |
Study Start Date : | December 2006 |
Actual Primary Completion Date : | January 2008 |
Actual Study Completion Date : | January 2008 |

Arm | Intervention/treatment |
---|---|
Experimental: Olopatadine 0.6% Nasal Spray
2 sprays each nostril twice daily
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Drug: Olopatadine 0.6% nasal spray
2 sprays each nostril twice daily |
Placebo Comparator: Placebo Nasal Spray
2 sprays each nostril twice daily
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Drug: Placebo Nasal Spray
2 sprays each nostril twice daily |
- Mean Response at Day 30 to the Patient-rated Relief Assessment Questionnaire [ Time Frame: day 30 ]Mean Patient-Rated Relief Assessment at Day 30. The patient-rated relief assessment (PRRA) was a 4-point scale with 1=Complete Relief; 2=Moderate Relief; 3=Mild Relief; and 4=No Relief.
- Average Number of Days of Rescue Medication Taken [ Time Frame: Month 1 through Month 12 ]

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Ages Eligible for Study: | 12 Years and older (Child, Adult, Older Adult) |
Sexes Eligible for Study: | All |
Accepts Healthy Volunteers: | No |
Inclusion Criteria:
- Patients with confirmed diagnosis of perennial allergic rhinitis who are 12 years and older
Exclusion Criteria:
- Age 11 years and younger

To learn more about this study, you or your doctor may contact the study research staff using the contact information provided by the sponsor.
Please refer to this study by its ClinicalTrials.gov identifier (NCT number): NCT00578331
United States, Texas | |
Waco | |
Waco, Texas, United States, 76712 |
Study Director: | Margaret Drake | Alcon Research |
Responsible Party: | Alcon Research |
ClinicalTrials.gov Identifier: | NCT00578331 |
Other Study ID Numbers: |
C-05-69 |
First Posted: | December 21, 2007 Key Record Dates |
Results First Posted: | February 3, 2010 |
Last Update Posted: | October 31, 2017 |
Last Verified: | February 2010 |
rhinitis perennial allergic rhinitis allergic rhinitis |
Rhinitis Rhinitis, Allergic Rhinitis, Allergic, Perennial Respiratory Tract Infections Infections Nose Diseases Respiratory Tract Diseases Otorhinolaryngologic Diseases Respiratory Hypersensitivity Hypersensitivity, Immediate Hypersensitivity Immune System Diseases Olopatadine Hydrochloride Anti-Inflammatory Agents, Non-Steroidal |
Analgesics, Non-Narcotic Analgesics Sensory System Agents Peripheral Nervous System Agents Physiological Effects of Drugs Anti-Inflammatory Agents Antirheumatic Agents Anti-Allergic Agents Histamine H1 Antagonists, Non-Sedating Histamine H1 Antagonists Histamine Antagonists Histamine Agents Neurotransmitter Agents Molecular Mechanisms of Pharmacological Action |