Skip to content

Real World Cohort Study of Xu' s Influenza Decoction in the Treatment of Influenza A Virus Infection

Real World Cohort Study of Xu' s Influenza Decoction in the Treatment of Influenza A Virus Infection

Status
Recruiting
Phases
Unknown
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2300070057
Enrollment
Unknown
Registered
2023-03-31
Start date
2022-11-20
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

Influenza A

Interventions

Integrative Medicine Group(retrospective):NA
Western Medicine Group(retrospective):NA
Integrative Medicine Group(prospective):NA
Healthy Control Group(prospective):NA

Sponsors

The First Affiliated Hospital of Zhejiang Chinese Medical University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
14 Years to 83 Years

Inclusion criteria

Inclusion criteria: 1.Retrospective study (1) Patients aged = 14 years. (2) Have the clinical manifestations of influenza. (3) Influenza A virus antigen test positive. (4) Treatment with oseltamivir and/or Xu's influenza decoction. 2. Prospective study (1) The course of disease = 48 h and body temperature = 38 °C. (2) At least one respiratory symptom ( nasal congestion, sore throat, cough ), and at least one systemic symptom (fever, headache, muscle pain, aversion to cold or sweating, fatigue ). (3) Influenza A virus antigen test positive. (4) Age = 18 years and = 65 years. (5) Patients informed and agreed to sign the informed consent.

Exclusion criteria

Exclusion criteria: 1. Retrospective study (1) In line with the ' critical case ' criteria, such as respiratory failure. (2) Patients with end-stage renal disease, malignant tumor and other serious basic diseases or mental diseases. (3) Patients with body temperature less than 37.3 °C on admission. (4) Patients who received influenza decoction treatment and increased traditional Chinese medicine > 5 flavors on its basis. (5) Course of disease less than 2 days. 2.Prospective study (1) In line with the ' critical case ' criteria, such as respiratory failure. (2) Pregnant or puerperal women. (3) Patients with end-stage renal disease, malignant tumor and other serious basic diseases or mental diseases. (4) Receive influenza vaccination within 12 months. (5) Allergic constitution or drug allergy (history). (6) has taken antiviral drugs or other Chinese medicine treatment of influenza.

Design outcomes

Primary

MeasureTime frame
Time to defervescence(retrospective);Cumulative antipyretic rate(retrospective);Immune cells and cytokines(perspective);curative effect of TCM syndromes(effective rate, perspective);

Secondary

MeasureTime frame
Blood routine and CRP(retrospective);Length of stay(retrospective);Medical costs(retrospective);Subgroup analysis on time to defervescence(retrospective);Symptom relief time(perspective);Secondary complications ( prospective );Blood routine and CRP (prospective );Length of stay(prospective);Medical costs(prospective);

Countries

China

Contacts

Public ContactShuyan Fu

The First Affiliated Hospital of Zhejiang Chinese Medical University

15967120645@163.com15967120645

Outcome results

None listed

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