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Effect of Jingfang mixture on influenza (Wind-Cold Syndrome)in elderly patients:a multicenterprospectivecohort study

Effect of Jingfang mixture on influenza (Wind-Cold Syndrome)in elderly patients:a multicenterprospectivecohort study

Status
Active, not recruiting
Phases
Phase 4
Study type
Observational
Source
ITMCTR
Registry ID
ITMCTR2024000443
Enrollment
Unknown
Registered
2024-09-17
Start date
2024-10-14
Completion date
Unknown
Last updated
2024-10-14

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

Conditions

Influenza

Interventions

Jingfang mixture high-dose plus Oseltamivir group:Jingfang mixture (po 20ml tid)
Oseltamivir(po 75mg tid)
Jingfang mixture low-dose plus Oseltamivir group:Jingfang mixture (po 10ml tid)
Oseltamivir grou:Oseltamivir(po 75mg tid)
Jingfang mixture low-dose group:Jingfang mixture (po 10ml tid)
Jingfang mixture high-dose group:Jingfang mixture (po 20ml tid)

Sponsors

Guangdong Provincial Chinese Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
65 Years to 130 Years

Inclusion criteria

Inclusion criteria: (1)Age =65 years old (2)Diagnosed as influenza (3)Diagnosed as Wind-Cold Syndrome (4)Prescription is in line with the medication regimen of protocol (5)Duration of illness =48 hours (6)Sign the informed consent form.

Exclusion criteria

Exclusion criteria: (1)Severe or critical influenza (2)Patients with other respiratory tract infections such as pharyngeal conjunctival feverherpanginapurulent tonsllitisetc. (3)Patients with influenza complicationsincluding bacterial sinusitisotitis mediabronchitispneumoniaetc. (4)Have regularly usse anti-influenza virus drugs within 48 hours before this visit (5)Pregnant and lactating women (6)Patents with immunocompromised diseasetumors and inmunosupresed or deficientsuch as long-term use of hormones or immunosuppressantshuman inmunodeficiency virus infetion (7)Patients with serious primary diseases of the heartbrainliverkidneyhematopoietic and other systems (8)Those who are allergic to the observed drugs and ingredients (9)Those who have participated in any other drug or device trials in the last one month (10)Those judged by other investigators to affect the observation and safety of drug efficacy.

Design outcomes

Primary

MeasureTime frame
Time to resolution of influenza symptoms;

Secondary

MeasureTime frame
Proportion of patients hospitalized dueto influenza progression;Proportion of patients who became critically ill with influenza;Incidence of influenza complications;Time for complete deferment of fever;Remission rate and duration of individual symptoms;TCM syndrome evaluation;Dosage and proportion of antipyretic analgesics;

Countries

China

Contacts

Public ContactZhongde Zhang

Guangdong Provincial Chinese Hospital

doctorzzd99@163.com81887233

Outcome results

None listed

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