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Clinical Study on the Intervention of Qingfei Decoction in Respiratory Symptoms of Viral Infection in Cancer Patients

Clinical and Mechanistic Study of Qingfei Decoction Intervention on Respiratory Symptoms of Viral Infection in Cancer Patients

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
ITMCTR
Registry ID
ITMCTR2024000758
Enrollment
Unknown
Registered
2024-12-01
Start date
2024-12-01
Completion date
Unknown
Last updated
2024-12-09

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

Conditions

Solid tumor

Interventions

control group:conventional treatment
observational group: Conventional treatment combined with Qingfei Decoction

Sponsors

Zhejiang Cancer Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 80 Years

Inclusion criteria

Inclusion criteria: 1. Patients diagnosed with solid tumors by histopathology; 2. Common respiratory viral infections confirmed by pathogen or antigen testing (respiratory syncytial virus adenovirus coronavirus influenza virus Epstein-Barr virus parainfluenza virus human metapneumovirus cytomegalovirus rhinovirus measles virus coxsackievirus etc.); 3. Presence of obvious respiratory symptoms cough severity score (CET = 8 points).

Exclusion criteria

Exclusion criteria: 1. Those allergic to the components of the Qingfei Heji; 2. Those with a history of chronic lung diseases (including bronchiectasis asthma chronic obstructive pulmonary disease chronic cough for more than 8 weeks lung cancer lung abscess respiratory bacterial infections etc.); 3. Current or former heavy smokers defined as a smoking index (number of smoking years multiplied by the number of cigarettes smoked per day) = 400; 4. Those unable to complete regular follow-ups; 5. Those with severe comorbidities or acute exacerbations of chronic diseases (such as acute heart failure); 6. Subjects who participated in or are currently participating in other clinical trials within one month prior to this study; 7. Those taking other traditional Chinese medicine during the study period.period.

Design outcomes

Primary

MeasureTime frame
Cough Examination Test(CET);

Secondary

MeasureTime frame
Degree of dyspnea (Revised British Medical Research Council dyspnea questionnaire);Pulmonary fibrosis assessment;Fatigue level rating;

Countries

China

Contacts

Public ContactZhang Aiqin

Zhejiang Cancer Hospital

zhanghaojianbb@163.com13777462976

Outcome results

None listed

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