Effect of NK cell therapy in COVID-19
Phase 1
Recruiting
- Conditions
- Condition 1: COVID-19. Condition 2: COVID-19. Condition 3: Viral pneumonia.COVID-19, virus identifiedCOVID-19, virus not identifiedOther viral pneumoniaU07.1U07.2J12.8
- Registration Number
- IRCT20200417047113N1
- Lead Sponsor
- Middle East Gene Therapy corporation
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Recruiting
- Sex
- All
- Target Recruitment
- 70
Inclusion Criteria
All COVID-19 patients confirmed by CT scan with possitive RT-PCR
Exclusion Criteria
Pregnancy or breastfeeding
Known HIV, HBV or HCV infection
Patients with malignant tumor, other serious systemic diseases and psychosis
Diabetic patients
Patients who are participating in other clinical trials
Study & Design
- Study Type
- interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Fever. Timepoint: Days 1, 3, 7, 14, and 28. Method of measurement: Thermometer.;Number of breathes per minute. Timepoint: Days 1, 3, 7, 14, and 28 after cell injection. Method of measurement: Records of the number of breaths in a minute by Nurse in 3 consecutive minutes.;Pulmonary volume. Timepoint: Days 7 and 14. Method of measurement: Spirometer.;Pulmonary capacity. Timepoint: Days 7 and 14. Method of measurement: Spirometer.;Airway resistance. Timepoint: Days 7 and 14. Method of measurement: Spirometer.;Lung elasticity. Timepoint: Days 7 and 14. Method of measurement: Spirometer.;Chest pressure. Timepoint: Days 7 and 14. Method of measurement: Spirometer.;Cough. Timepoint: Days 1, 3, 7, 14, and 28 after cell injection. Method of measurement: Records in questionnaire by nurse according to defined qualitative criteria.;Skin disorders. Timepoint: Days 1, 3, 7, 14, and 28. Method of measurement: Records in questionnaire by nurse according to defined qualitative criteria.
- Secondary Outcome Measures
Name Time Method ymphopenia. Timepoint: Day 7. Method of measurement: Complete blood count.