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Honey effect on cough alleviatio

Not Applicable
Conditions
Common Cold.
Acute nasopharyngitis
Registration Number
IRCT201110247882N1
Lead Sponsor
Hormozgan University of Medical Sciences(HUMS)
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Complete
Sex
All
Target Recruitment
126
Inclusion Criteria

The patients's age is two to five years old; Acute cough is the chief complaint;The symptoms of viral upper respiratory tract infection are the only concomitant symptoms [fever (oral temperature from 37.8to 38.5 or axillary temp from 37.2 to 37.9) rhinorrhea , sneezing, blocked nose, sore throat, cough, mild headache, restlessness, hoarseness];The patient has been brought to clinic at first or second day of begining cough;The patient has not bacterial infections symptoms of upper respiratory tract (moderate to high fever, sever sore throat with painful swallowing, severe headache, nausea, vomiting, abdominal pain, ...);The patient has not the symptoms of lower respiratory tract infection (high fever, chills, dyspnea, malaise, pleuritic chest pain, tachypnea, retraction); There are not associated infections such as otitis and sinusitis; Allergy is not considered ( associated symptoms such as itchy eye & nose, history of repeating similar symptoms, a history of prolonged cold periods, positive family history; The patient has not signs of Reactive Airway Disease (wheezing, shortness of breath,pressure or tightness feeling in chest , tachypnea, tachycardia); The parents have not begun any drug before coming to clinic . Exclusion criteria were: Onset of otitis or sinusitis symptoms; Onset of symptoms of lower respiratory tract involvement; Adding a bacterial infection, (purulent nasal discharge, high fever, difficulty breathing, Periorbital edema, facial pain); Not using of recommended treatments; Adding other drugs to recommended treatment; Non-coordinated reports of persons who take care of patients.

Exclusion Criteria

Not provided

Study & Design

Study Type
interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
umber of Night cough. Timepoint: Before intervention, 48 h after intervention. Method of measurement: Visual scale of the number of coughs.;Severity of night cough. Timepoint: Before intervention, 48 h after intervention. Method of measurement: Visual scale of severity of coughs.;The number of daily cough. Timepoint: Before intervention, 48 h after intervention. Method of measurement: Visual scale of the number of coughs.;Severity of daily cough. Timepoint: Before intervention, 48 h after intervention. Method of measurement: Visual scale of severity of cough.
Secondary Outcome Measures
NameTimeMethod
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