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Evaluation of Efficacy and Safety of Levocetirizine to Subjects With Perennial Allergic Rhinitis to House Dust Mites

NCT ID: NCT00521131

Last Updated: 2013-12-16

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

COMPLETED

Clinical Phase

PHASE4

Total Enrollment

453 participants

Study Classification

INTERVENTIONAL

Study Start Date

2002-09-30

Study Completion Date

2003-05-31

Brief Summary

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Evaluation of Efficacy and Safety of Levocetirizine to Subjects With Perennial Allergic Rhinitis to House Dust Mites

Detailed Description

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Conditions

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Rhinitis Allergic Perennial

Keywords

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Levocetirizine dihydrochloride Xyzal tablets

Study Design

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Allocation Method

RANDOMIZED

Intervention Model

PARALLEL

Primary Study Purpose

TREATMENT

Blinding Strategy

DOUBLE

Interventions

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Levocetirizine dihydrochloride

Intervention Type DRUG

Eligibility Criteria

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Inclusion Criteria

* male or female ≥ 12 years
* suffering from a perennial allergic rhinitis to house dust mites for at least 2 years
* positive skin test or positive Radio-Allergo-Sorbent-Test for house dust mites
* the mean of the T4SS evaluated in the evening over the last 24 hours of the selection period was ≥ 5

Exclusion Criteria

* seasonal allergic rhinitis likely to change significantly the symptoms of the subject
* an ear, nose or throat (ENT) infection during the two weeks preceding initial visit
* asthma requiring corticosteroid treatment
* atopic dermatitis or urticaria requiring an antihistamine treatment or the administration of oral or topical corticosteroids
* associated ENT disease
Minimum Eligible Age

12 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

No

Sponsors

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UCB Pharma

INDUSTRY

Sponsor Role lead

Principal Investigators

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UCB Clinical Trial Call Center

Role: STUDY_DIRECTOR

UCB Pharma

Other Identifiers

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A00333

Identifier Type: -

Identifier Source: org_study_id