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Comparative effectiveness and safety of ribavirin plus interferon-alpha, lopinavir/ritonavir plus interferon-alpha and ribavirin plus lopinavir/ritonavir plus interferon-alphain in patients with mild to moderate novel coronavirus pneumonia

Comparative effectiveness and safety of ribavirin plus interferon-alpha, lopinavir/ritonavir plus interferon-alpha and ribavirin plus lopinavir/ritonavir plus interferon-alphain in patients with mild to moderate novel coronavirus pneumonia

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2000029387
Enrollment
Unknown
Registered
2020-01-29
Start date
2020-01-25
Completion date
Unknown
Last updated
2020-03-02

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

Conditions

Novel Coronavirus Pneumonia (COVID-19)

Interventions

arm A:Ribavirin + Interferon alpha-1b
arm B:lopinavir / ritonavir + interferon alpha-1b
arm C:Ribavirin + LPV/r+Interferon alpha-1b

Sponsors

Chongqing Public Health Medical Center
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 65 Years

Inclusion criteria

Inclusion criteria: (1) 18–65 years of age; (2) Diagnosed as mild to moderate COVID-19; (3) Be willing to sign informed consent; (4) The clinical assessment and condition of the subject does not influence the completion of the study.

Exclusion criteria

Exclusion criteria: (1) Patients are diagnosed as a case of severe NCIP; (2) Patients are pregnant or breastfeeding women; (3) Patients have aspartate aminotransferase (AST) or alanine aminotransferase (ALT) > 5×UNL or creatinine clearance <50 ml / min; (4) Patients are allergic or intolerant to the proposed antiviral therapeutic drugs; (5) Patients are HIV-positive; (6) Patients with hemoglobin disease (7) Patients have severe heart disease, brain disease, lung disease, kidney disease, tumor or other severe systemic diseases; (8) Patients are not willing to provide signed informed consent.

Design outcomes

Primary

MeasureTime frame
The time to 2019-nCoV RNA negativity in patients;

Secondary

MeasureTime frame
mortality on day 28;The rate of negative 2019-nCoV RNA results at day 14;the rate of aggravation;the rate of adverse events ;The rate of discontinuations due to adverse events;

Countries

China

Contacts

Public ContactYaokai Chen

Chongqing Public Health Medical Center

yaokaichen@hotmail.com+86 023-65481658

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 18, 2026