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Clinical Study on Mortality Reduction in Acute Exacerbation of Idiopathic Pulmonary Fibrosis through Integrated Traditional Chinese and Western Medicine Therapy

Clinical Study on Mortality Reduction in Acute Exacerbation of Idiopathic Pulmonary Fibrosis through Integrated Traditional Chinese and Western Medicine Therapy

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ITMCTR
Registry ID
ITMCTR2025001917
Enrollment
Unknown
Registered
2025-10-15
Start date
2025-12-31
Completion date
Unknown
Last updated
2025-11-17

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

Conditions

Acute Exacerbation of Idiopathic Pulmonary Fibrosis (AE-IPF)

Interventions

treatment group:On the basis of guideline-directed treatment the treatment group was administered Kangxian Huanji Granule
control group:On the basis of guideline-directed treatment the Kangxian Huanji Granule placebo was administered

Sponsors

The Second Affiliated Hospital of Tianjin University of Traditional Chinese Medicine
Lead Sponsor

Eligibility

Sex/Gender
All
Age
40 Years to 85 Years

Inclusion criteria

Inclusion criteria: 1.Hospitalized patients meeting the diagnostic criteria for Acute Exacerbation of Idiopathic Pulmonary Fibrosis (AE-IPF); 2.Patients meeting the standards of Traditional Chinese Medicine (TCM) syndrome differentiation; 3.Age range: 40 to 85 years; 4.Voluntary acceptance of treatment and signing of informed consent.

Exclusion criteria

Exclusion criteria: 1.Patients with other pulmonary diseases such as chronic obstructive pulmonary disease (COPD) lung cancer active pulmonary tuberculosis bronchiectasis or pulmonary embolism; 2.Patients with severe cardiovascular and cerebrovascular diseases (e.g. malignant arrhythmia unstable angina acute myocardial infarction heart function of grade 3 or above stroke or cerebral hemorrhage); 3.Patients with liver diseases such as cirrhosis or secondary portal hypertension bleeding caused by esophageal and gastric varices or kidney diseases requiring dialysis or kidney transplantation or those with abnormal liver and kidney function (ALT AST BUN exceeding 1.5 times the upper limit of normal or blood Cr exceeding the upper limit of normal); 4.Patients who have been taking hormones and/or immunosuppressants for a long time; 5.Patients with impaired consciousness or various psychiatric disorders who are unable to communicate normally; 6.Pregnant or lactating women or those with a recent pregnancy plan; 7.Patients who have participated in other clinical trials within the past month; 8.Patients with known allergies to any trial drugs or their components.

Design outcomes

Primary

MeasureTime frame
case fatality rate;

Secondary

MeasureTime frame
Mechanical Ventilation Rate;CRP;ATAQ-IPF;Immunoglobulin;PCT;Pulmonary Function;Ferritin;Chest HRCT;SGRQ;mMRC;blood gas analysis;length of stay;T Cell Subsets;KL-6;

Countries

China

Contacts

Public ContactFENG JIHONG

The Second Affiliated Hospital of Tianjin University of Traditional Chinese Medicine

1194542291@qq.com13820337614

Outcome results

None listed

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