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Evaluation of the effectiveness of Nigel-7 capsule and black seed mixture on corona

Phase 2
Recruiting
Conditions
COVID-19.
U07.2 COVID-19, virus not identified, COVID-19
U07.2
Registration Number
IRCT20160131026298N6
Lead Sponsor
Bagheiat-allah University of Medical Sciences
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Recruiting
Sex
All
Target Recruitment
80
Inclusion Criteria

Male or female patients 18 years old and older with Coronavirus Disease 2019 (COVID-19)
Ground glass view at low-dose CT scan
Consciously completed consent form completed by the patient or the patient's supervisor

Exclusion Criteria

History of pulmonary malignancy
History of asthma or COPD
History of Disabling disease or malignancy
Liver or kidney disorders

Study & Design

Study Type
interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Measurement of cough severity. Timepoint: Day 1 before and at the end of treatment. Method of measurement: Cough scoring form.;Severity of shortness of breath. Timepoint: Day 1 before and at the end of treatment. Method of measurement: Shortness Of Breath With Daily Activity (SOBDA) Questionnaire.;Lung radiologic changes. Timepoint: At beginning and end of the study. Method of measurement: Chest CT scan.
Secondary Outcome Measures
NameTimeMethod
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