The effect of SOVODAK in the treatment of COVID-19 patients
Phase 3
Recruiting
- Conditions
- COVID-19.B34.2Coronavirus infection, unspecified
- Registration Number
- IRCT20200403046926N1
- Lead Sponsor
- Mazandaran University of Medical Sciences
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Recruiting
- Sex
- All
- Target Recruitment
- 60
Inclusion Criteria
Diagnosis by CT scan with clinical symptoms
Consent to attend the study
Lymphocyte count less than 1100
Positive CRP test
Exclusion Criteria
History of kidney failure
Pregnancy
Amiodarone consumer
Study & Design
- Study Type
- interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Symptoms ending. Timepoint: During the study. Method of measurement: Clinical examination.;Lymphopenic Status. Timepoint: Before the intervention and the seventh day. Method of measurement: Counting lymphocytes.;C-reactive protein Status. Timepoint: Before the intervention and the seventh day. Method of measurement: C-reactive protein serological test.;Saturation of Peripheral Oxygen. Timepoint: Before the intervention and the seventh day. Method of measurement: Pulseimetry.
- Secondary Outcome Measures
Name Time Method eed hospitalization. Timepoint: Depending on the situation. Method of measurement: Depending on the patient's condition.