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Trials / Completed

CompletedNCT00783237

Onset of Effect of Mometasone Nasal Spray in Induced Allergic Rhinitis (Study P03431)

Onset of Action of Mometasone Furoate Nasal Spray vs. Placebo in Induced Allergic Rhinitis

Status
Completed
Phase
Phase 4
Study type
Interventional
Enrollment
340 (actual)
Sponsor
Organon and Co · Industry
Sex
All
Age
12 Years
Healthy volunteers
Not accepted

Summary

This was a single-dose study to determine the time it takes for mometasone furoate nasal spray to go in effect, after a single dose of 2 sprays per nostril. Patients who are eligible were exposed to ragweed pollen for 3 hours on one or two occasions. Patients who experienced adequate symptoms during the pollen exposure phase came back for a Treatment Phase visit. During the Treatment Phase visit, patients were exposed to ragweed pollen for 2 hours and then received either mometasone or placebo nasal spray. Symptom evaluations began on the patients every hour for the next 11 hours.

Conditions

Interventions

TypeNameDescription
DRUGMometasoneMometasone Furoate Nasal Spray, single dose of 200 mcg (2 sprays per nostril)
DRUGPlaceboPlacebo nasal spray, single dose of 2 sprays per nostril

Timeline

Start date
2003-12-01
Primary completion
2004-02-21
Completion
2004-02-21
First posted
2008-10-31
Last updated
2024-08-15

Source: ClinicalTrials.gov record NCT00783237. Inclusion in this directory is not an endorsement.

Onset of Effect of Mometasone Nasal Spray in Induced Allergic Rhinitis (Study P03431) (NCT00783237) · Clinical Trials Directory