Skip to content

A real-world study to evaluate the efficacy and safety of tocilizumab and baritinib in the treatment of severe novel coronavirus pneumonia in China.

A real-world study to evaluate the efficacy and safety of tocilizumab and baritinib in the treatment of severe novel coronavirus pneumonia in China.

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2300073887
Enrollment
Unknown
Registered
2023-07-24
Start date
2023-09-01
Completion date
Unknown
Last updated
2023-07-30

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Topics initiated by our researchers

Interventions

Tocilizumab + standard treatment group:NA
baricitinib + standard treatment group:NA

Sponsors

Shenzhen Second Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to No maximum

Inclusion criteria

Inclusion criteria: ( 1 ) Age > 18 years ; ( 2 ) PCR-positive COVID-19 infection confirmed by any specimen ( e.g., respiratory tract, blood, urine, feces, other body fluids ) ; ( 3 ) Confirmed as pneumonia by CT scan or chest X-ray ;

Exclusion criteria

Exclusion criteria: ( 1 ) Death within 24 hours of admission ( 2 ) Patients requiring mechanical ventilation within 24 hours of admission ( 3 ) Active tuberculosis infection, suspected active bacterial, fungal, viral or other infection ( except for COVID-19 )

Design outcomes

Primary

MeasureTime frame
Cumulative proportion of all-cause deaths or patients requiring mechanical ventilation as of day 28;

Secondary

MeasureTime frame
On the 28 th day, the median time of discharge or ' preparation for discharge ' or the median time of clinical status improvement;

Countries

China

Contacts

Public ContactWang Meiying

Shenzhen Second Hospital

wmy99wmy99@163.com+86 137 2376 9919

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 4, 2026