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NCT00724698 Clinical Trial

Evaluation of Desloratadine When Used in Patients With Either Allergic Rhinitis or Chronic Idiopathic Urticaria

Rhinitis Clinical Trial

— Aerius  

Official title:
Post-marketing Surveillance of the Safety, Tolerability and Efficacy of Desloratadine Tablet Among Filipino Patients

Clinical Trial Details — Status: Completed

Administrative data
NCT number NCT00724698
Other study ID # P04706
Secondary ID
Status Completed
Phase
First received
Last updated
Start date October 2005
Est. completion date December 2007

Study information
Verified date February 2022
Source Organon and Co
Contact n/a
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

Eligible patients will be prescribed Desloratadine 1 tablet of 5 mg once daily. Patients will be asked to follow-up for a final visit after 14 days (Day 15) where the safety, tolerability and clinical efficacy will be measured.

Recruitment information / eligibility
Status Completed
Enrollment 3011
Est. completion date December 2007
Est. primary completion date December 2007
Accepts healthy volunteers No
Gender All
Age group 12 Years and older
Eligibility Inclusion Criteria: - Outpatient men or women, age 12 years and above. - Diagnosis of Allergic Rhinitis or Chronic Idiopathic Urticaria Exclusion Criteria: - Known hypersensitivity to Desloratadine. - Pregnancy or lactation

Study Design

Related Conditions & MeSH terms

Intervention

Drug:
• Desloratadine
Desloratadine 5 mg once daily

Locations
Country Name City State
n/a

Sponsors (1)
Lead Sponsor Collaborator
Organon and Co

Outcome
Type Measure Description Time frame Safety issue
Primary Adverse Events Number of adverse events reported Final Visit (Day 15)
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