COVID-19. Coronavirus infection, unspecified
Conditions
Interventions
Intervention 1: Intervention group: Kaletra 200 mg/50 mg tablet every 12 hours + hydroxychloroquine 200 mg tablets every 12 hours + herbal medicine containing sage, hofariqun and fennel (5 ml 3 times
Sponsors
Mazandaran University of Medical Sciences
Eligibility
Sex/Gender
All
Age
18 Years to No maximum
Inclusion criteria
Inclusion criteria: Temperatures above 2 degrees Lymphocyte count less than 2 CRP positive Respiratory symptoms Symptoms of pulmonary involvement in CT scan Satisfaction to participate in the study Age older than 18 years
Exclusion criteria
Exclusion criteria: Oral intolerance Pulmonary disease
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Fever. Timepoint: Every day for 7 days. Method of measurement: termometer.;Lymphocyte count. Timepoint: Before and 7 days after intervention. Method of measurement: Cell counter device.;Erythrocyte sedimentation rate. Timepoint: Before and 7 days after intervention. Method of measurement: ESR device. | — |
Secondary
| Measure | Time frame |
|---|---|
| Pneumonia. Timepoint: Before and 14 days after intervention. Method of measurement: CT-Scan. | — |
Countries
Iran (Islamic Republic of)
Contacts
Public ContactFarhang Babamahmoodi
Mazandaran University of Medical Sciences
Outcome results
None listed