Effect of Bromhexine Hydrochloride on patients with COVID-19
Phase 3
Recruiting
- Conditions
- Condition 1: Patients with COVID-2019. Condition 2: .COVID-19, virus identifiedU07.1
- Registration Number
- IRCT20200317046797N4
- Lead Sponsor
- Tabriz University of Medical Sciences
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Recruiting
- Sex
- All
- Target Recruitment
- 60
Inclusion Criteria
Patients with COVID-19-induced pneumonia confirmed with PCR
Patients or authorized family members volunteered to participate in this study and signed informed consent.
Both genders
18 to 80 years old
Exclusion Criteria
Patients who are participating in other drug clinical trials
Pregnant or lactating women
Patient with active thrombotic event
Patients with severe respiratory failure
Study & Design
- Study Type
- interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Hospitalization days. Timepoint: At baseline and discharge time. Method of measurement: Counting the days.;Need for mechanical ventilation. Timepoint: From baseline to discharge time. Method of measurement: Observation and documents.;Condition of discharge (death or recovery). Timepoint: End of hospitalization. Method of measurement: Observation and documents.;Period of mechanical ventilation. Timepoint: End of hospitalization. Method of measurement: Documents of hospitalization.
- Secondary Outcome Measures
Name Time Method