At a glance
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A Methodology Study to Assess Cough Counts in Subjects With Acute Upper Respiratory Tract Infections
In Brief
A clinical study evaluating Placebo, Guaifenesin, and 1 other intervention for Infection. Completed, enrolled 265 participants across 2 sites.
Detailed Summary
The objectives of this study are: a) to assess the feasibility and sensitivity of manually count cough bouts over a 4-hour period; b) to assess the effects of buckwheat honey and guaifenesin 400 mg immediate release tablets compared to placebo on the frequency and severity of acute cough due to upper respiratory tract infection and c) to evaluate the correlation between cough bout frequency and subjective assessments of cough severity. The hypotheses to be tested is that 10 ml of buckwheat honey and 400 mg of immediate release guaifenesin will significantly reduce the frequency and severity of cough compared to placebo over a 4-hour evaluation period.
Study Details
Timeline
Interventions
One placebo tablet administered orally as a single dose
One 400 mg immediate release tablet administered orally as a single dose
10 mL administered orally as a single dose