post infection cough.
Conditions
Interventions
Intervention 1: Intervention group: the coded syrup will be administrated each 8h 10 cc for 1 week. Intervention 2: Control group: the coded syrup will be administrated each 8h 10 cc for 1 week.
Sponsors
Tehran University of Medical Sciences
Eligibility
Sex/Gender
All
Age
18 Years to 75 Years
Inclusion criteria
Inclusion criteria: All hospitalized patient with post-infection cough
Exclusion criteria
Exclusion criteria: Participating in another study Known case of DM 1 & 2, seizure, pulmonary disease like asthma and COPD Drug history of phenytoin, phenobarbital, gentamicin and venlafaxin Symptoms like hemoptysis which may have special diagnosis Pregnancy and lactation Drug which may cause cough like ACEI History of Rhinitis and allergy, GERD, smoking Hypersensitivity to any ingredient of herbal syrup
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Cough score in visual analogue scale. Timepoint: Day 1,2,7,14. Method of measurement: visual analogue scale.;Cough score in simplified cough score. Timepoint: Day 1,2,7,14. Method of measurement: Simplified cough score.;Score in cough symptom score. Timepoint: Day 1,2,7,14. Method of measurement: Cough symptom score. | — |
Secondary
| Measure | Time frame |
|---|---|
| Data laboratory changes. Timepoint: Daily. Method of measurement: Data laboratory from blood sample. | — |
Countries
Iran (Islamic Republic of)
Contacts
Public ContactMarziyeh Heydari
Tehran University of Medical Sciences
Outcome results
None listed