Phase
Condition
Common Cold
Rhinitis, Allergic, Perennial
Allergy
Treatment
N/AClinical Study ID
Ages > 12 All Genders
Study Summary
Eligibility Criteria
Inclusion
Inclusion Criteria:
Comply with all the purposes and procedures of the study by signing and dating the ICown free will. In the case of minors, the document should be signed and dated by theparent or legal guardian;
Have age over 12 years, regardless of gender, ethnicity or social class;
Present clinical status of perennial allergic rhinitis from mild to moderate;
Present clinical status with at least 12 months of evolution;
Submit the examination of IgE elevation (above 100KU / L).
Exclusion
Exclusion Criteria:
Have participated in any experimental study or have taken any experimental drug in the 12 months preceding the start of the study;
Pregnant or lactating women;
Have made use of:
Intranasal or systemic corticosteroids in the month before inclusion;
Intranasal cromolyn in the two weeks preceding inclusion;
Intranasal or systemic decongestants in the 03 days preceding inclusion;
Intranasal antihistamines or systemic in the 03 days preceding the survey;
Loratadine in the 10 days preceding the survey.
have any disease or anatomical abnormality in the upper airways which could jeopardizethe analysis of data, for example, tumors or severe septal deviations;
History of smoking in the 03 months preceding the inclusion;
History of alcohol or illicit drugs;
History of liver disease or kidney disease;
Electric current asthma or gift last year;
Table of uncontrolled hypertension;
Patients with heart disease or who use drugs for the cardiovascular system that issuffering interference of the drugs studied, for example, β-blockers;
Patients with flu-like symptoms or fever of unknown origin, defined current or withinlast 07 days;
Clinical diagnosis of rhinitis is not that kind of allergic and perennial;
Be patient with sensitivity to loratadine, pseudoephedrine sulfate, or any componentsof the formula;
Estimated travel or displacement of the southeast for more than 50% of monitoring.
Study Design
Study Description
Connect with a study center
Lal Clínica Pesquisa E Desenvolvimento Ltda
Valinhos, Sao Paulo 13270-245
BrazilSite Not Available
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