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Clinical study on Fuzheng Tongluo Formula in the treatment of idiopathic pulmonary fibrosis

Clinical study on Fuzheng Tongluo Formula in the treatment of idiopathic pulmonary fibrosis

Status
Recruiting
Phases
Early Phase 1
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2000037392
Enrollment
Unknown
Registered
2020-08-28
Start date
2020-10-01
Completion date
Unknown
Last updated
2020-10-19

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

Conditions

Idiopathic pulmonary fibrosis

Interventions

Sponsors

Shuguang Hospital Affiliated to Shanghai University of TCM
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: 1. Patients who meet the IPF diagnostic criteria of Western medicine; 2. Patients who meet the TCM diagnostic criteria of kidney deficiency and collateral stasis type; 3. Patients aged 50-85 years, both male and female; 4. Patients with good compliance; 5. Patients who voluntarily participate in the experiment and sign informed consent.

Exclusion criteria

Exclusion criteria: 1. Acute exacerbation or fulminant patients or late critical patients; 2. Patients with severe primary diseases such as cardiovascular, liver, kidney and hematopoietic system and mental illness; 3. Patients with other acute diseases such as infection, fever and bleeding; 4. Pregnant or lactating women; 5. Patients who are known to be allergic to test drug ingredients; 6. Patients who participated in other clinical studies in recent 3 months; 7. Patients who are not willing to receive trial treatment.

Design outcomes

Primary

MeasureTime frame
HRCT;TCM syndrome integral and single main symptom integral;

Secondary

MeasureTime frame
six minutes walk distance;St. George's respiratory questionnaire;modified medical research council;Pulmonary function;Blood gas analysis;Serum cytokines;

Countries

China

Contacts

Public ContactWei Zhang

Shuguang Hospital Affiliated to Shanghai University of TCM

zhangw1190@sina.com+86 13023153956

Outcome results

None listed

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