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The effect of Nintedanib in post-COVID-19 lung fibrosis: an observational study

The effect of Nintedanib in post-COVID-19 lung fibrosis: an observational study

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
TCTR
Registry ID
TCTR20220426001
Enrollment
29
Registered
2022-04-26
Start date
2022-04-29
Completion date
Unknown
Last updated
2026-08-03

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

Conditions

Patients with COVID-19 pneumonia and lung fibrosis COVID-19 Pneumonia Lung fibrosis Nintedanib Antifibrotic Oxygenation Chest radiograph Mortality

Interventions

Patients with COVID-19 pneumonia and lung fibrosis treated with nintedanib at least 5 days,Patients with COVID-19 pneumonia and lung fibrosis treated with standand medications (no nintedanib)
Treatment,Treatment
Nintedanib group,Control group

Sponsors

Faculty of Medicine, Thammasat University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to No maximum

Inclusion criteria

Inclusion criteria: 1. Age 18 years or more, 2. Diagnosis of COVID-19 confirmed by RT-PCR test for SAR-CoV-2, 3. Diagnosis of pneumonia confirmed by chest imaging, 4. Hospital admission at Thammasat University Hospital, 5. Treatment with nintedanib or standard treatment

Exclusion criteria

Exclusion criteria: None

Design outcomes

Primary

MeasureTime frame
Oxygenation improvement at 60 days after treatment Number (%),Chest X-ray improvement at 60 days after treatment Number (%),Mortality rate at 60 days after treatment Number (%)

Secondary

MeasureTime frame
Length of hospital stay at the end of study days,SpO2/FiO2 ratio difference between before and after treatment at the end of study number

Countries

Thailand

Contacts

Public ContactNarongkorn Saiphoklang

Faculty of Medicine, Thammasat University

M_narongkorn@hotmail.com6629269794

Outcome results

None listed

Source: TCTR (via WHO ICTRP) · Data processed: Aug 9, 2026