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Clinical observation and study of pirfenidone combined with dextromethorphan on idiopathic pulmonary fibrosis

Clinical observation and study of pirfenidone combined with dextromethorphan on idiopathic pulmonary fibrosis

Status
Recruiting
Phases
Phase 4
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2000037602
Enrollment
Unknown
Registered
2020-08-29
Start date
2020-01-01
Completion date
Unknown
Last updated
2020-11-02

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

Conditions

Interstitial lung disease

Interventions

1:Dextromethorphan+Pirfenidone
2:Pirfenidone

Sponsors

Tianjin Medical University General Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 75 Years

Inclusion criteria

Inclusion criteria: 1. The patients who met the IPF diagnostic criteria of ATS / ERS / JRS / ALAT in 2018: HRCT accorded with UIP type and possible UIP type; 2. Patients aged 18 to 75 years; 3. Those patients who fully understand the treatment purpose and grouping method, and those who may have adverse reactions such as gastrointestinal discomfort, liver dysfunction, skin damage and so on, and sign the informed consent form.

Exclusion criteria

Exclusion criteria: 1. Patients with allergy or intolerance to pirfenidone and dextromethorphan; 2. Patients who had used glucocorticoid or immunosuppressant within one month before enrollment; 3. Patients who have been used for a long time (>=2 weeks) with fibrogenic drugs such as amiodarone; 4. Patients with typical CTD-ILD.

Design outcomes

Primary

MeasureTime frame
Chest HRCT;Pulmonary Function;

Secondary

MeasureTime frame
blood routine, Liver Function,Renal Function;

Countries

China

Contacts

Public ContactJing Feng

Tianjin Medical University General Hospital

fengjing1974@163.com+86 13920500251

Outcome results

None listed

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