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Efficacy evaluation of naproxat mesylate in patients with chronic kidney disease complicated with novel coronavirus infection

Efficacy evaluation of naproxat mesylate in patients with chronic kidney disease complicated with novel coronavirus infection

Status
Active, not recruiting
Phases
Phase 4
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2300069312
Enrollment
Unknown
Registered
2023-03-13
Start date
2023-04-01
Completion date
Unknown
Last updated
2023-05-29

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

Conditions

chronic kidney disease

Interventions

intervention group:Naproxat mesylate + standard treatment group for COVID-19 infection
control group:standard treatment group for COVID-19 infection

Sponsors

West China Hospital of Sichuan University
Lead Sponsor

Eligibility

Sex/Gender
Male
Age
18 Years to No maximum

Inclusion criteria

Inclusion criteria: 1. Age >= 18 years old; 2. Hospitalized patients who meet the criteria for diagnosis and treatment of chronic kidney disease; 3. Those who tested positive for COVID-19 nucleic acid or antigen within 3 days before randomization.

Exclusion criteria

Exclusion criteria: 1. Serious hematological diseases, malignant tumors, and organ transplants; 2. Mental illness or other reasons can not cooperate with the treatment; 3. Allergic constitution, known allergic to the test drug (naphthalmositat mesylate) and its excipients; 4. Women who are pregnant, planning to become pregnant recently, or lactating; 5. Participants who have participated in other clinical trials within the last 1 month; 6. Researchers believe that there are other unsuitable candidates for inclusion.

Design outcomes

Primary

MeasureTime frame
Clinical improvement rate;

Secondary

MeasureTime frame
Clinical recovery time;All-cause mortality at 14 and 28 days;

Countries

China

Contacts

Public ContactZhang Ling

West China Hospital of Sichuan University

zhangling_crrt@163.com+86 18980601985

Outcome results

None listed

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