COVID-19
Conditions
Keywords
COVID-19
Brief summary
This study aims to compare the efficacy and safety of Methylprednisolone versus Tocilizumab in improving clinical outcomes and reducing the need for ventilator support in COVID-19 patients with moderate COVID-19 disease at risk for complications of cytokine storm. Approximately 310 participants hospitalized with COVID-19 in UMMC, Hospital Sungai Buloh, Hospital Kuala Lumpur and Hospital Tuanku Jaafar will be enrolled into this study. Eligible participants will be selected based on a set of clinical, laboratory and radiological parameters indicative of early stages of CRS and lung function decline prior to being randomized at a ratio of 1:1 to receive either Tocilizumab or Methylprednisolone. Participants will be monitored daily for clinical and laboratory parameters, and at 48 hours, switched to the alternate study arm should they manifest signs and symptoms indicative of decompensation.
Interventions
DRUGTocilizumab
IV infusion
DRUGMethylprednisolone
IV infusion
Sponsors
University of Malaya
Study design
Allocation
RANDOMIZED
Intervention model
CROSSOVER
Primary purpose
TREATMENT
Masking
NONE
Eligibility
Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No
Inclusion criteria
1\) Hospitalised symptomatic COVID-19 patients 2( Presence of clinical and radiological signs of progressive disease, AND laboratory evidence indicative of risk for cytokine storm complications. All patients participating in this clinical trial must meet the following inclusion criteria: 1. Hospitalised symptomatic COVID-19 patients 2. Presence of clinical and radiological signs of progressive disease, AND laboratory evidence indicative of risk for cytokine storm complications: Clinical: Dyspnoea OR RR\>20 breaths/min AND O2 sat \<93% on RA OR increasing need for O2 supplementation to maintain O2 sat \>95% on RA WITH Radiological: CXR or CT indicative of pneumonia OR worsening findings over time AND Laboratory: CRP levels \>60 OR an increase of CRP \>20 over 12 hours WITH an increasing ferritin level OR declining lymphocyte counts 3. Age \> 18 years and able to give consent
Exclusion criteria
Patients will be excluded if any of the following conditions apply: 1. Known sensitivity/allergy to TCZ or other monoclonal antibodies 2. AST/ALT\>5 times UNL, platelet counts \<50,000 or neutrophil counts \<500 3. Active TB 4. Pregnant 5. Receipt of mechanical ventilation 6. Has received other immunomodulatory drugs (including TCZ) in the past for the treatment of other conditions 7. Individuals, in the opinion of the investigator, where progression to death is imminent and inevitable in the next 24 hours irrespective of treatment provision or who have signed a DNR. 8. Participating in other clinical trials (subject to approval) 9. Any serious medical condition or abnormal clinical laboratory tests which in the judgement of the investigator may compromise patient safety should he/she participate in the study.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| The proportion of patients requiring mechanical ventilation | Through study completion, and average of 6 months |
| Mean days of ventilation | Through study completion, and average of 6 months |
Secondary
| Measure | Time frame |
|---|---|
| The proportion of patients requiring ICU admission | Through study completion, and average of 6 months |
| Overall 28-day survival | 28 day from baseline |
| Change in symptom severity assessed by the World Health Organization (WHO) Coronavirus Disease 2019 (COVID19) ordinal scale measured daily up to 7 days from baseline | 7 days from baseline |
| Duration of hospital and ICU stay | Through study completion, and average of 6 months |
Countries
Malaysia
Contacts
Primary ContactAdeeba Kamarulzaman, MBBS
Backup ContactReena Rajasuriar, PhD
Outcome results
None listed