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The effect of SOVODAK in the treatment of COVID-19 patients

Phase 3
Recruiting
Conditions
COVID-19.
B34.2
Coronavirus 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
NameTimeMethod
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
NameTimeMethod
eed hospitalization. Timepoint: Depending on the situation. Method of measurement: Depending on the patient's condition.
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