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Clinical characteristics, therapeutic strategies and mechanism of pulmonary fibrosis secondary to novel coronavirus infection

Clinical characteristics, therapeutic strategies and mechanism of pulmonary fibrosis secondary to COVID-19

Status
Unknown
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2300076539
Enrollment
Unknown
Registered
2023-10-11
Start date
2023-11-01
Completion date
Unknown
Last updated
2024-06-03

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

Conditions

Pulmonary fibrosis secondary to COVID-19

Interventions

Pirfenidone group:Based on the basic treatment given to the control group, the initial dose of pirfenidone was titrated gradually to 400mg tid from 100mg tid for maintenance treatment.
Nidanib group:In addition to the basic treatment given to the control group, the patients were given Nidanib 100-150mg bid maintenance therapy according to their weight and tolerance.
Control group:Only conventional oxygen therapy and pulmonary rehabilitation therapy were given, in addition to basic therapeutic measures such as relieving cough and reducing phlegm drugs were allowed

Sponsors

Fujian Provincial Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 100 Years

Inclusion criteria

Inclusion criteria: 1. Aged >= 18 years old; 2. Patients with novel coronavirus infection: According to the Diagnosis and Treatment Protocol for Novel Coronavirus Infection (Trial 10th Edition) released in January 2023, patients diagnosed with novel coronavirus infection after admission; 3. Pulmonary fibrosis was found in the patient's computed tomography of chest (determined jointly by two specialists above the deputy director of the imaging department).

Exclusion criteria

Exclusion criteria: 1. COVID-19 infection without pneumonia; 2. Mild to medium COVID-19 patients with no abnormal changes in chest images reexamined 1 month later; 3. Patients who died before the start of follow-up; 4. Patients who cannot cooperate because of mental disorders, dementia or other reasons; 5. Patients with pulmonary fibrosis before COVID-19 infection; 6. Patients with advanced tumors.

Design outcomes

Primary

MeasureTime frame
Glycochain antigen KL-6;Lung function;Chest Computed Tomography scan;

Secondary

MeasureTime frame
Dyspnea mMRC scale;SF-36;6-minute walking test;Inflammatory cytokines (TNF-a, IL-8, IL-17A, IL-17D, etc.);

Countries

China

Contacts

Public ContactHongru Li

Fujian Provincial Hospital

muzi131122@fjmu.edu.cn+86 186 5030 8626

Outcome results

None listed

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