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Effect of Bromhexine Hydrochloride on patients with COVID-19

Phase 3
Recruiting
Conditions
Condition 1: Patients with COVID-2019. Condition 2: .
COVID-19, virus identified
U07.1
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
NameTimeMethod
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
NameTimeMethod
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