COVID 19. COVID-19, virus identified
Conditions
Interventions
Intervention 1: Control group: Without placebo. Intervention 2: Intervention group: first intervention group, anticoagulant. ? the patients will be started on unfractional heparin. Blood sample will t
Sponsors
Tabriz University of Medical Sciences
Eligibility
Sex/Gender
All
Age
15 Years to 70 Years
Inclusion criteria
Inclusion criteria: COVID patients with P/F ratio less than 100 D.dimer more than 3000 without response to other medications
Exclusion criteria
Exclusion criteria: Active bleeding Platelet less than 30000 Without any contraindication for thrombolytic therapy
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Improve of oxygenasion. Timepoint: From first to 6th days of study. Method of measurement: Arterial blood gas.;Improve SOFA score. Timepoint: From first to 6th days of study. Method of measurement: Questionnaire.;Improve compliance. Timepoint: From first to 6th days of study. Method of measurement: Ventilator parameter.;Decrease d.Dimer level. Timepoint: From first to 6th days of study. Method of measurement: Blood sample. | — |
Countries
Iran (Islamic Republic of)
Contacts
Public ContactFarid Rashidi
Tabriz University of Medical Sciences
Outcome results
None listed