Center for Environmental Medicine, Asthma, and Lung Biology
Chapel Hill, North Carolina, 27599, United States
NCT Number: NCT01114581
The purpose of this research study is to explore the mechanism of action of Mucinex, an oral, over-the-counter, FDA approved expectorant in patients with acute respiratory tract infections.
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Notify Me18 year–65 year
All sexes
Interventional
Phase 2
Chapel Hill, North Carolina, 27599, United States
Healthy volunteers accepted: No
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
Exclusion criteria
Mucinex 1200mg (Guaifenesin) given as 2,600mg tablets, one time on day 1 of the study
Placebo given as 2 tablets
Time frame: 3 hours following inhalation of radioactive tracer particles
Percentage of inhaled radioactive tracer (Ave180Clear)
Time frame: 3 hours following dose administration
Time frame: Within 10 days of developing symptoms associated with a respiratory tract infection
Reckitt Benckiser LLC
Industry
Acronym: MCC/CC
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View the official ClinicalTrials.gov record (opens in a new tab)This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.
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