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The clinic research for Liu Shen capsule in the treatment of seasonal influenza

A multicenter, double-blind, randomized, placebo-controlled clinical trial to evaluate efficacy and safety of Liu Shen capsule in the treatment of seasonal influenza

Status
Recruiting
Phases
Phase 4
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR1900027401
Enrollment
Unknown
Registered
2019-11-12
Start date
2019-10-31
Completion date
Unknown
Last updated
2019-11-18

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

Conditions

seasonal influenza

Interventions

control group:placebo

Sponsors

The First Affiliated Hospital of Guangzhou Medical University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 65 Years

Inclusion criteria

Inclusion criteria: (1) Aged 18 to 65 years; (2) Patients whose rapid influenza diagnostic tests (RIDTs) result is positive, and consistent with the clinical diagnosis of influenza; (3) Patients whose onset of symptoms occurred =38.0 degree C and any influenza symptom); (4) Patients whose temperature (armpit) >= 38.0 degree C in the past 24 hours; (5) At least one of the following systemic symptoms: headache, muscle aches, chills, sweating, fatigue; (6) At least one of the folloeing respiratory symptoms: cough, sore throat, stuffy nose; (7) Patients who sign the informed consent form freely and voluntarily.

Exclusion criteria

Exclusion criteria: (1) Lateral and anteroposterior chest radiography or chest CT scan results showed bronchitis, pneumonia, pleural effusion, interstitial lesions, etc.; (2) White blood cell count (WBC) > 10.0 x 10^9/L, or 30kg/m^2; (8) Diabetic; Patients with severe underlying illness, such as hematopathy, severe COPD (FEV1/EVC = 3ULN, TBIL >= 1.5ULN); Severe renal insufficiency (SCr >177µmol/L or 2mg/dL); Congestive heart failure(NYHA III-IV); Psychopath; (9) Patients used anti-influenza drugs within 7 days prior screening (such as oseltamivir, zanamivir, peramivir, favipiravir, arbidol, amantadine, rimantadine etc.); Or Chinese medicine with antiviral effect was used within 7 days prior screening(such as Jin Hua Qing Gan, Lian Hua Qing Wen, Qing Kai Ling, Shu Feng Jie Du, Yin Qiao Jie Du, Sang Ju Gan Mao, Yin Huang, Kang Bing Du Kou Fu Ye etc);Or Liu Shen Capsule was used within 7 days prior screening; (10) Allergic constitution patients,who are allergic to the drugs which used in this research; (11) Lactating or pregnant female, or planning for pregnancy within 6 months after screening, or urine pregnancy test was positive; Family planning male, or planning for sperm donation; (12) Immunodeficiency (such as malignant tumor, solid organ or bone marrow transplant, aids, using immunosuppressive drugs within 3 months prior screening); (13) Suspected or existing history of alcohol and drug abuse; (14) Participated in any other clinical treatment within 3 months prior to screening; (15) Patients who have had acute respiratory infection, otitis media, or sinusitis within 2 weeks prior to screening; (16) Patients who have been vaccinated against seasonal flu or the H1N1 flu; (17) The researchers consider the patients are not suitable.

Design outcomes

Primary

MeasureTime frame
The AUC of influenza symptom score;

Secondary

MeasureTime frame
each symptom score;Time to alleviation of individual symptom;Proportion of patients whose symptoms has been alleviated at each time point;defervescence time;defervescence rate;time to return to preinfluenza health status;propotion of patients who return to preinfluenza health status;Time to cessation of viral shedding;negative rate of virus;Inflammatory Factors;the frequency and the dosage of sea water nasal irrigations;propotion of using antibiotic;complication incidence;

Countries

China

Contacts

Public ContactYe Feng

The First Affiliated Hospital of Guangzhou Medical University

yefeng@gird.cn+86 020-83062837

Outcome results

None listed

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