Skip to content

Establishment of a real-world follow-up database for interstitial lung disease and exploration of new diagnosis and treatment models

Establishment of a real-world follow-up database for interstitial lung disease and exploration of new diagnosis and treatment models

Status
Recruiting
Phases
Unknown
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR1900024810
Enrollment
Unknown
Registered
2019-07-29
Start date
2019-08-28
Completion date
Unknown
Last updated
2026-01-05

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

Conditions

Interstitial lung disease

Interventions

Observational group:None

Sponsors

West China Hospital, Sichuan University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 90 Years

Inclusion criteria

Inclusion criteria: 1. Adults aged over 18 years; 2. Diagnosis meets the diagnostic criteria for IPF, CTD-ILD, or CTD; 3. Suspected cases must be confirmed by a multidisciplinary team within the research group; 4. Expected survival time is more than 1 year.

Exclusion criteria

Exclusion criteria: 1. Comorbidities that may significantly affect the prognosis of CTD-ILD/IPF, such as pneumoconiosis, silicosis, or malignant tumors; 2. Pregnant or breastfeeding women; 3. Participants who are unable to comply with the study protocol.

Design outcomes

Primary

MeasureTime frame
Changes of PFT;Total exacerbations;Blood tests (Complete Blood Count, Biochemistry, C-Reactive Protein, Erythrocyte Sedimentation Rate, Procalcitonin, Interleukin-6, Immune-related tests, Tumor Necrosis Factor-alpha);Bronchoalveolar Lavage Fluid (BALF) Cytomics and Genomics;Cryobiopsy Related Information (Surgical Procedure, Pathology Results of the Specimen, Follow-up Information for Three Days Post-Procedure);Dyspnea Scales and Classification (mMRC Questionnaire, Borg Dyspnea Scale);Cough Assessment (Cough Symptom Score, Cough VAS Score);King's Brief Interstitial Lung Disease questionnaire;Six-Minute Walk Test;Exhaled Nitric Oxide, FeNO;

Secondary

MeasureTime frame
Survival time;Symptom evaluation;forms of 'acute exacerbation';Grades of HRCT;The MOS item short from health survey;Changes of inflammation markers;Pulmonary artery hypertension;BMI;

Countries

China

Contacts

Public ContactFengming Luo

West China Hospital, Sichuan University

fengmingluo@outlook.com+86 189 8060 1355

Outcome results

None listed

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