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Clinical study for Celebrex in the treatment of novel coronavirus pneumonia (COVID-19)

Clinical study for Celebrex in the treatment of novel coronavirus pneumonia (COVID-19)

Status
Recruiting
Phases
Early Phase 1
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2000031630
Enrollment
Unknown
Registered
2020-04-05
Start date
2020-02-17
Completion date
Unknown
Last updated
2020-04-06

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:Celebrex capsules 200mg / time twice a day for 7 days
control group:routine treatment

Sponsors

Guangzhou Eighth People's Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to No maximum

Inclusion criteria

Inclusion criteria: 1. The nucleic acid of novel coronavirus 2019 was positive or the virus gene was highly homologous to the known new coronavirus. 2. The patient has fever or / and pneumonia; 3. Aged >=18 years old.

Exclusion criteria

Exclusion criteria: 1. Have a clear history of celecoxib allergy; 2. Serious nausea, vomiting, diarrhea and other clinical manifestations affect the oral or absorption of the drug; 3. Taking drugs that may interact with celecoxib at the same time; 4. Patients with serious basic diseases, such as heart disease (including history of angina pectoris or coronary heart disease of myocardial infarction, atrioventricular block), lung, kidney, liver, etc., or mental diseases that cannot be treated together; 5. History of peptic ulcer; 6. Pregnant and lactating women; 7. Suspected or confirmed that there is still a history of alcohol, drug abuse or drug abuse; 8. Participated in other drug trials in the past month.

Design outcomes

Primary

MeasureTime frame
Prostaglandin E2;

Countries

China

Contacts

Public ContactHong wenxin

Guangzhou Eighth People's Hospital

winsonhong@126.com+86 13729834533

Outcome results

None listed

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