Clinical Trials Directory

Trials / Completed

CompletedNCT00789152

The Effect of Desloratadine and Levocetirizine on Nasal Obstruction (Study P03609)

The Effects of Desloratadine and Levocetirizine on Nasal Obstruction in Subjects With Induced Allergic Rhinitis in the VCC Assessed Clinically and With Nasal Rhinomanometry and Nasal Flowmetry

Status
Completed
Phase
Phase 3
Study type
Interventional
Enrollment
81 (actual)
Sponsor
Organon and Co · Industry
Sex
All
Age
18 Years – 45 Years
Healthy volunteers
Not accepted

Summary

This was a study to measure the ability of desloratadine and levocetirizine to decrease nasal obstruction in subjects who had study-induced allergic rhinitis. Study participants had allergic rhinitis symptoms induced in a Vienna Challenge Chamber and then received desloratadine or levocetirizine for 8 days. After at least a 10 to 35-day washout period (time when no drug is given), subjects received the opposite treatment for 8 days. Subjects had their total nasal symptom measured.on the 8th day of each treatment period.

Conditions

Interventions

TypeNameDescription
DRUGdesloratadinedesloratadine 5 mg daily x 8 days
DRUGlevocetirizinelevocetirizine 5 mg daily x 8 days

Timeline

Start date
2003-12-01
Primary completion
2004-05-01
Completion
2004-05-01
First posted
2008-11-11
Last updated
2024-08-15

Source: ClinicalTrials.gov record NCT00789152. Inclusion in this directory is not an endorsement.