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The clinical research of combined use of hydroxycoumarin in the treatment of novel coronavirus infection

The clinical research of combined use of hydroxycoumarin in the treatment of novel coronavirus infection

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2500101350
Enrollment
Unknown
Registered
2025-04-23
Start date
2023-12-13
Completion date
Unknown
Last updated
2025-04-28

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

Conditions

Novel coronavirus infection

Interventions

Conventional therapies:Patients with COVID-19 are treated with symptomatic treatment, antiviral therapy, immunotherapy, respiratory support, and intensive care.
Conventional treatment is combined with oxymethacoumarin:On the basis of symptomatic treatment, antiviral therapy, immunotherapy, respiratory support, and intensive care, patients were treated with hy

Sponsors

People's Hospital of Ningxia Hui Autonomous Region
Lead Sponsor

Eligibility

Sex/Gender
All
Age
14 Years to No maximum

Inclusion criteria

Inclusion criteria: 1.Be over 14 years old, and with no gender limitation; 2.Patients confirmed with novel coronavirus infection, using the nasopharyngeal swab; 3.The level of hyaluronic acid in serum is greater than 100ng/ml.

Exclusion criteria

Exclusion criteria: 1.Pations with severe non-infectious pulmonary disease, including lung tumor,pulmonary atelectasis,pulmonary embolism,pulmonary eosinophilic infiltration,pulmonary vasculitis; 2.Patients who has severe liver and kidney dysfunction, for example; ALT and AST exceed the upper limit of normal value by more than 10 times; the serum creatinine exceed the upper limit of normal value by more than 1.5 times; the total bilirubin exceed the upper limit of normal value by more than 2 times; 3.Patients with biliary obstruction; 4.Other patients that investigators consider they do not suitable for this trial, or the investigators believe that there may be any conditions that increase the risk of participants or interfere with the clinical trial.

Design outcomes

Primary

MeasureTime frame
Hyaluronan levels;SARS-CoV-2 viral load;

Secondary

MeasureTime frame
Lymphocyte restoration condition;Changes in inflammatory factor levels (Interleukin-6, Ferritin, C-reactive protein, Erythrocyte Sedimentation Rate, and Procalcitonin);

Countries

China

Contacts

Public ContactZhuan Bing

People's Hospital of Ningxia Hui Autonomous Region

zhuanb518@163.com+86 187 0951 8179

Outcome results

None listed

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