Evaluation of the effectiveness of Nigel-7 capsule and black seed mixture on corona
IRCT; 2020-09-08; TrialID: IRCT20160131026298N6
Clinical Trial Register
| ICTRP | ID: ictrp-IRCT20160131026298N6
ABSTRACT
Condition
COVID-19.U07.2 COVID-19, virus not identified, COVID-19;U07.2
Intervention
Intervention 1 Intervention group Intervention groups will be two ones. Patients in the intervention group will receive the intervention drug (three capsules a day and ten grams of black seed mixture daily) that is made by Talaye sabze tooba company; in addition to the routine treatment (Azithromycin 250 mg daily for 10 days and Naproxen 250 mg twice a day for 10 days) . Intervention 2 Control group The control group will receive the routine treatment (Azithromycin 250 mg daily for 10 days and Naproxen 250 mg twice a day for 10 days) .Primary outcome:
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.Criteria
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
Collection:
Clinical trial registers
Database:
ICTRP
Year:
2020
Document Type:
Clinical Trial Register
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