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Association study of genetic polymorphisms with idiopathic pulmonary fibrosis

Association study of genetic polymorphisms with idiopathic pulmonary fibrosis

Status
Recruiting
Phases
Unknown
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR-ROC-16007721
Enrollment
Unknown
Registered
2016-01-07
Start date
2016-01-01
Completion date
Unknown
Last updated
2017-04-18

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

Conditions

Idiopathic pulmonary fibrosis

Interventions

Control:No
IPF:No

Sponsors

the Second Affiliated Hospital of Harbin Medical University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
15 Years to 90 Years

Inclusion criteria

Inclusion criteria: All recruited patients with IPF fully met the ATS/ERS diagnostic criteria, such as glass attenuation and the coarseness of fibrosis. Diagnosis of IPF was further supported by history, physical examination, chest X-ray, high-resolution CT scan, arterial blood gas analysis, pulmonary function test and transbronchial lung biopsy.

Exclusion criteria

Exclusion criteria: Clear etiology of pulmonary fibrosis, allergic lung disease, cancer and other lung diseases

Design outcomes

Primary

MeasureTime frame
FOXP3;NLRP3;OR2B11;FAM154B;ARHGEF28;IL17F;MMP12;MMP9;CCDC22;—

Secondary

MeasureTime frame
IL21R;sle related;IRF5;TLN1;—

Countries

China

Contacts

Public ContactZhang Lili
zhanglili_80@126.com+86 18845870460

Outcome results

None listed

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