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The effect of Licorice lozenges on chronic cough treatment

Phase 3
Conditions
Chronic Cough.
Cough-chronic
Registration Number
IRCT2015022421220N1
Lead Sponsor
Shiraz University of Medical Sciences
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Complete
Sex
All
Target Recruitment
60
Inclusion Criteria

patients between 18-70 years old; with resistant idiopathic chronic cough for more than 8 weeks; written informed consent to participate in the project
Exclusion criteria: any allergic reaction to the drug; asthma; COPD; GERD; Rhinitis; pregnancy and lactation; hypertension; arrhythmia; Zollinger syndrome; mineralocorticoid and anticoagulants consumers; pregnancy during the study; the drug lost more than three doses; increasing in blood pressure during the study

Exclusion Criteria

Not provided

Study & Design

Study Type
interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Cough severity. Timepoint: Baseline. Method of measurement: Leicester cough questionnaire.
Secondary Outcome Measures
NameTimeMethod
Cough severity. Timepoint: 2 weeks after treatment and 2 weeks after the end of intervention. Method of measurement: Leicester Cough Questionnaire.
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