The purpose of this study is to evaluate the efficacy of the Naridrin in improving nasal congestion.
Open label, randomized, multicenter clinical study. Maximal experiment duration: 2 days; 2 visits. Safety and efficacy evaluation
Study Type
INTERVENTIONAL
Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
NONE
Enrollment
292
Faculdade de Medicina do ABC
Santo André, São Paulo, Brazil
Relief of Nasal Congestion
Relief of nasal congestion will be measured on a scale of 0 to 3 (0 = without congestion and 3 total congestion)
Time frame: 2 days
Adverse Events
Safety of the drug will be assessed by observation of adverse events monitored for the type, frequency and intensity during the days of the follow-up. The evaluation of the heart frequency will also be a safety parameter.
Time frame: 2 days
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