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Surveillance and Prevention Strategies for Influenza Viruses in Fever Clinics

Surveillance and Prevention Strategies for Influenza Viruses in Fever Clinics

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2600121599
Enrollment
Unknown
Registered
2026-04-01
Start date
2026-04-01
Completion date
Unknown
Last updated
2026-04-14

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

Conditions

Influenza, fever, sore throat, runny nose, etc

Interventions

Sponsors

Shanghai General Hospital
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: 1. Part 1 (Epidemiological Characteristics Analysis) Inclusion Criteria: (1) The patient visited the fever clinic of our hospital between March 1, 2023, and February 29, 2024. (2) Presented with fever (body temperature >= 37.3°C) accompanied by at least one of the following influenza-like symptoms: 1) Systemic symptoms: headache, dizziness, fatigue, general muscle/joint soreness, loss of appetite, etc. 2) Upper respiratory symptoms: nasal congestion, runny nose, cough, sputum production, etc. 3) Throat-related discomfort: sore throat, itchy throat, dry throat, etc. (3) Completed influenza A/B virus antigen testing on the day of the visit. 2. Part 2 (Case-Control Study) Inclusion Criteria: (1) Influenza-Positive Group: In addition to meeting criteria (1) and (2) in Part 1, the patient must have a positive influenza virus antigen test result and a complete set of routine blood test results. (2) Influenza-Negative Group: In addition to meeting criteria (1) and (2) in Part 1, the patient must have a negative influenza virus antigen test result and a complete set of routine blood test results.

Exclusion criteria

Exclusion criteria: 1. Part 1 (Epidemiological Characteristics Analysis) Exclusion Criteria: (1) Exclusion of duplicate records of patients revisiting for influenza-like symptoms after a confirmed diagnosis (e.g., non-influenza viral infection). (2) Incomplete medical records with missing or illegible key information (such as age, gender, test results, visit time). (3) Invalid or indeterminate antigen test results. 2. Part 2 (Case-Control Study) Exclusion Criteria: (1) Subjects meeting any of the exclusion criteria in Part 1. (2) Patients in either the case or control group lacking complete routine blood test results.

Design outcomes

Primary

MeasureTime frame
Overall influenza virus positive detection rate;Proportion of influenza A and B types;

Secondary

MeasureTime frame
Demographic (gender, age) and seasonal (month) distribution characteristics of influenza-positive cases;Differences in clinical symptoms, blood routine indicators, and chest imaging findings between influenza-positive and negative cases;

Countries

China

Contacts

Public ContactCao Yangwei

Shanghai General Hospital

019119cyw@shgh.cn+86 21 63246117

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Apr 17, 2026