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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT00453583
Other study ID # A00420
Secondary ID
Status Completed
Phase N/A
First received March 28, 2007
Last updated December 13, 2013
Start date March 2007
Est. completion date January 2008

Study information

Verified date May 2012
Source UCB Pharma
Contact n/a
Is FDA regulated No
Health authority European Union: European Medicines AgencySouth Korea: Korea Food and Drug Administration (KFDA)India: Ministry of HealthMexico: National Institute of Public Health, Health SecretariatSpain: Spanish Agency of Medicines
Study type Observational

Clinical Trial Summary

This is a non-interventional retrospective data collection study from children aged from 2 to 12 years old diagnosed with an allergy and who received a treatment consisting of an H1-antihistamine. The period of last taken medication will be observed to evaluate the global satisfaction of the parents and physician for this last treatment.


Recruitment information / eligibility

Status Completed
Enrollment 4581
Est. completion date January 2008
Est. primary completion date January 2008
Accepts healthy volunteers No
Gender Both
Age group 2 Years to 12 Years
Eligibility Inclusion Criteria:

- Children from 2-12 included

- History of allergy

- Used an Antihistamine within market authorization

Exclusion Criteria:

- Child not yet treated for the presented allergy

Study Design

Time Perspective: Retrospective


Related Conditions & MeSH terms


Locations

Country Name City State
United States UCB Pharma Smyrna Georgia

Sponsors (1)

Lead Sponsor Collaborator
UCB Pharma

Country where clinical trial is conducted

United States, 

Outcome

Type Measure Description Time frame Safety issue
Primary Parent satisfaction on a 11-point scale duration of the study No
Secondary Physician satisfaction on an 11-point scale duration of the study No
Secondary Efficacy, tolerability and global satisfaction duration of the study No
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