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A medical records based study for risk assessment and treatment timing of invasive fungal infection in novel coronavirus pneumonia (COVID-19) critical patients

Risk assessment and treatment timing of invasive fungal infection in critically ill covid-19 patients: medical records based study

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2000030717
Enrollment
Unknown
Registered
2020-03-11
Start date
2020-04-01
Completion date
Unknown
Last updated
2020-03-16

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

Exposed group:Prophylactic antifungal therapy
Control group:Diagnostic antifungal therapy

Sponsors

Tongji Hospital, Tongji Medical College, Huazhong University of Science and Technology, Wuhan, China
Lead Sponsor

Eligibility

Sex/Gender
All
Age
14 Years to 90 Years

Inclusion criteria

Inclusion criteria: 1. confirmed critically ill covid-19; 2. grouping criteria: meet the clinical risk factor combination criteria for invasive candidiasis in critically ill patients proposed by ostrosky-zeichner et al in 2009: (1) the length of stay in ICU exceeds 4 days; (2) in line with two of the following three conditions: broad-spectrum antibiotics; Central venous catheterization; Mechanical ventilation; (3) meeting one of the following six criteria: total parenteral nutrition (day 1 to day 3); Dialysis (1-3 days); Major surgery or pancreatitis or immunosuppression or glucocorticoids (within 7 days).

Exclusion criteria

Exclusion criteria: 1. If the patient received any antifungal treatment (excluding fluconazole or up to 7 days of selective digestion purification therapy) within 14 days prior to randomization, or if there was evidence of IFI; 2. aged < 14 years; 3. pregnant or lactating women; 4. allergy or hypersensitivity to any research drug or excipient; 5. participate in another clinical study or treat with an experimental drug 28 days prior to registration or use an accompanying drug therapy that the investigator considers likely to interfere with the study target.

Design outcomes

Primary

MeasureTime frame
14-days mortality;28-days mortality;

Countries

China

Contacts

Public ContactMinghao Fang

Department of Emergency, Tongji Hospital

fangmh@tjh.tjmu.edu.cn+86 15071157405

Outcome results

None listed

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