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Establishment of an Early Warning and Prevention System for Drug-Induced Lung Injury

Establishment of an Early Warning and Prevention System for Drug-Induced Lung Injury

Status
Active, not recruiting
Phases
Early Phase 1
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2600126055
Enrollment
Unknown
Registered
2026-06-03
Start date
2026-07-01
Completion date
Unknown
Last updated
2026-06-08

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

Conditions

drug-induced lung injury

Interventions

experimental set:None
Clinical pilot verification group:None

Sponsors

West China Hospital of Sichuan University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 75 Years

Inclusion criteria

Inclusion criteria: 1. Aged 18–75 years, ECOG PS 0–2; 2. Patients planned to initiate or currently receiving high-risk pulmonary injury medications (e.g., specific antineoplastic agents, antirheumatic drugs, cardiovascular drugs, etc.); 3. Expected survival >=6 months, with complete baseline clinical assessment data (including HRCT imaging, pulmonary function tests, and laboratory examinations, etc.); 4. Major organ function essentially normal, meeting standard indications for primary disease and high-risk medications.

Exclusion criteria

Exclusion criteria: 1. History of confirmed severe interstitial lung disease, pulmonary fibrosis, or current severe active pulmonary infection; 2. Severe active pulmonary infection within 4 weeks prior to enrollment with incomplete radiological resolution; 3. Severe coagulation disorders or other conditions contraindicating/refusing blood, sputum, or other biological specimen collection; 4. Severe claustrophobia, inability to lie supine, or other objective limitations precluding high-resolution CT (HRCT) examination; 5. Other malignancies besides the primary disease that are not effectively controlled; 6. Female patients during pregnancy or lactation.

Design outcomes

Primary

MeasureTime frame
Pulmonary function parameters;Sensitivity;specificity;Area Under the Receiver Operating Characteristic Curve;

Countries

China

Contacts

Public ContactBingwen Zou

West China Hospital of Sichuan University

zoubingwen81@163.com+86 28 85421479

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Jun 11, 2026