A Trial of Lopinavir–Ritonavir in Adults Hospitalized with Severe Covid-19
Chinese Academy of Medical Sciences & Peking Union Medical College
Abstract
No therapeutics have yet been proven effective for the treatment of severe illness caused by SARS-CoV-2.
) of less than 300 mm Hg. Patients were randomly assigned in a 1:1 ratio to receive either lopinavir-ritonavir (400 mg and 100 mg, respectively) twice a day for 14 days, in addition to standard care, or standard care alone. The primary end point was the time to clinical improvement, defined as the time from randomization to either an improvement of two points on a seven-category ordinal scale or discharge from the hospital, whichever came first.
Citation impact
- FWCI
- 135.88
- Percentile
- 100%
- References
- 24
Authors
65- BCBin CaoCorresponding
Chinese Academy of Medical Sciences & Peking Union Medical College
- YWYeming Wang
Chinese Academy of Medical Sciences & Peking Union Medical College
- DWDanning Wen
Chinese Academy of Medical Sciences & Peking Union Medical College
- WLWen Liu
Chinese Academy of Medical Sciences & Peking Union Medical College
- JWJingli Wang
Chinese Academy of Medical Sciences & Peking Union Medical College
Topics & keywords
- Lopinavir
- Medicine
- Ritonavir
- Lopinavir/ritonavir
- Confidence interval
- Hazard ratio
- Randomization
- Randomized controlled trial
- Good health and well-being