TOCILIZUMAB - An Option for Patients With COVID-19 Associated Cytokine Release Syndrome; A Single Center Experience

PHASE4CompletedINTERVENTIONAL
Enrollment

93

Participants

Timeline

Start Date

May 12, 2020

Primary Completion Date

June 12, 2020

Study Completion Date

June 12, 2020

Conditions
Covid19
Interventions
DRUG

Tocilizumab

"Participants received an initial dose calculated as per the body weight (8mg/kg) maximum 800mg/dose) over 1 hour, followed by up to three additional doses if required as per the response after the first dose with 8 hours intervals. Predefined Parameters of disease severity were assessed 12 to 24 hourly. Injection Paracetamol 1g was administered before infusion. The response of the participants after Tocilizumab administration was recorded based on clinical parameters (Oxygen requirement, Fever, Need for invasive positive pressure ventilation), biochemical parameters (D-dimers, C-reactive protein (CRP), Ferritin, Lactate dehydrogenase (LDH) levels), Chest X-ray findings, and Repeated PCR test for COVID-19. Any side effects noted after administration of TOCILIZUMAB were recorded.~Any side effects noted after administration of TCZ/ Corticosteroid were recorded."

Trial Locations (1)

54000

Fatima Memorial Hospital College of Medicine & Dentistry, Lahore

All Listed Sponsors
lead

FMH College of Medicine and Dentistry

OTHER

NCT04730323 - TOCILIZUMAB - An Option for Patients With COVID-19 Associated Cytokine Release Syndrome; A Single Center Experience | Biotech Hunter | Biotech Hunter