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Study of Pinavir / Ritonavir Tablets (Trade Name: Kelizhi) Combined with Xiyanping Injection for Novel Coronavirus Pneumonia (COVID-19)

Study of Pinavir / Ritonavir Tablets (Trade Name: Kelizhi) Combined with Xiyanping Injection for Novel Coronavirus Pneumonia (COVID-19)

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2000030218
Enrollment
Unknown
Registered
2020-02-25
Start date
2020-01-22
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

Experimental group of ordinary COVID-19:Lopinavir / ritonavir tablets combined with Xiyanping injection
Control group of ordinary COVID-19:Keep ritonavir/ritonavir treatment
Experimental group of severe COVID-19:Lopinavir / ritonavir tablets combined with Xiyanping injection

Sponsors

Fifth People's Hospital of Ganzhou
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to No maximum

Inclusion criteria

Inclusion criteria: (1) Aged >=18 years; (2) Novel coronavirus pneumonia patients diagnosed by pathogenic testing; (3) The patient himself participated in the study voluntarily, agreed and signed the informed consent.

Exclusion criteria

Exclusion criteria: (1) Meet the diagnostic criteria for severe new-type coronavirus infection pneumonia; (2) Severe primary diseases that affect survival, including: uncontrolled malignant tumors, hematological diseases, and HIV that have not been metastasized in multiple places; (3) Obstructive pneumonia, pulmonary interstitial fibrosis, alveolar proteinosis, and allergic alveolitis caused by lung tumors; (4) Women who are breastfeeding or pregnant; (5) Those who are known to be allergic to the ingredients contained in the research medication, or patients with allergies; (6) Those who have continued to use immunosuppressive agents or organ transplants in the past 6 months; (7) Patients who have participated in other drug clinical trials within 3 months before the screening test; (8) The investigator judges that he or she cannot complete or should not participate in the study (expected death within 48 hours, and the patient refuses active treatment)

Design outcomes

Primary

MeasureTime frame
Clinical recovery time;Pneumonia Severity Index (PSI) score;

Countries

China

Contacts

Public ContactXie Liangdong

Fifth People's Hospital of Ganzhou

2590410004@qq.com+86 13707077997

Outcome results

None listed

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