Official Title
Comparison of the Efficacy and Safety of Two Corticosteroid Regimens in the Treatment of Diffuse Lung Disease After Coronavirus Disease 2019 (COVID-19) Pneumonia
Brief Summary

A proportion of patients with COVID-19 pneumonia have a prolonged course of illness. Some of these patients continue to have considerable respiratory symptoms or persistent hypoxemia. The CT abnormalities in these patients are often a combination of ground-glass opacities and patchy multifocal consolidation consistent with a pattern of OP. In several patients, these radiologic abnormalities persist. As with other forms of OP, patients with post-COVID OP or post COVID diffuse lung disease (PC-DLD) may benefit from treatment with oral glucocorticoids. The ideal dose of glucocorticoids for treating PC-DLD is unknown. In this study, the investigatros aim to compare the efficacy and safety of a medium dose and a low dose of prednisolone (as the initial dose) for the treatment of post-COVID. diffuse lung disease.

Detailed Description

A proportion of patients with COVID-19 pneumonia (with or without ARDS) have a prolonged
course of illness. Some of these patients continue to have considerable respiratory symptoms
or persistent hypoxemia. The CT abnormalities in these patients are often a combination of
ground-glass opacities and patchy multifocal consolidation consistent with a pattern of OP.
In several patients, these radiologic abnormalities persist even after the symptoms of active
COVID-19 have subsided and swabs from the upper respiratory tract for SARS-CoV-2 have turned
negative. Such patients may be classified as having a secondary form of OP, namely
post-infectious OP. Some of the patients also start developing signs of fibrosis.

As with other forms of OP, patients with post-COVID OP or post COVID diffuse lung disease
(PC-DLD) may benefit from treatment with oral glucocorticoids.

Glucocorticoids may be a double-edged sword in this clinical situation. Steroids reduce
inflammation associated with OP with a resultant resolution of symptoms, improvement in gas
exchange (resulting in the resolution of hypoxemia), and potentially preventing the
progression of early parenchymal abnormalities to irreversible fibrosis. However, they are
associated with adverse effects such as hyperglycemia, delayed viral clearance, and increased
susceptibility to infections. The ideal dose of glucocorticoids for treating PC-DLD is
unknown. As PC-DLD is likely to get recognised early (much earlier than the average duration
between onset of symptoms and diagnosis in other forms of OP, i.e., about 3-6 months), there
is a possibility a lower intensity of glucocorticoids may be sufficient for treatment than
the usual regimens, with the advantage of lesser adverse effects. A previous retrospective
study that compared two regimens (higher dose intensity [DI] of glucocorticoids alone vs.
glucocorticoids at a lower dose intensity along with clarithromycin), however, found that a
complete radiologic response was higher in the prednisone alone (higher DI) group (81% vs.
63%) than in the combination group (with a lower DI of prednisone). Statistical significance
was however not achieved (p=0.38), mainly due to the small sample size.

The investiagtors hypothesize that in PC-DLD a higher intensity (i.e., starting with a medium
dose of prednisolone) will be more effective than a lower dose intensity (i.e., starting with
a low dose of prednisolone) of glucocorticoids in effecting a radiologic response at six
weeks.

Completed
Post COVID-19 Diffuse Lung Disease

Drug: Medium dose prednisolone

Same as arm description

Drug: Low dose prednisolone

Same as arm description

Eligibility Criteria

Inclusion Criteria:

- Diagnosed to have COVID-19 by means of a real-time reverse transcription polymerase
chain reaction (rRT-PCR) test performed on a respiratory (upper or lower respiratory)
sample or the detection of COVID-19 antigen

- Having significant respiratory symptoms (cough and breathlessness) or persistent
hypoxemia or oxygen desaturation on exercise and CT chest showing residual changes of
post-COVID parenchymal involvement of any extent OR having CT chest showing residual
changes of post-COVID parenchymal involvement >20% of the lung parenchyma on visual
inspection of the scans between 3-8 weeks of the onset of symptoms of COVID-19

- Willing to participate in the study

Exclusion Criteria:

- Receiving ventilatory or respiratory support (invasive or non-invasive mechanical
ventilation or high flow nasal cannula) or supplemental oxygen with FiO2>0.35

- Requiring intensive care due to acute COVID-19 pneumonia or its complications

- Having a known lung parenchymal lung disease before the onset of COVID-19

- Pregnant or lactating women

- Having absolute contraindication for prednisolone in a dose of 40 mg/day (this
includes untreated glaucoma, uncontrolled diabetes mellitus, signs of an uncontrolled
or untreated infection or sepsis, pulmonary mycosis, untreated severe psychiatric
disorders)

- Unwilling to provide informed consent

Eligibility Gender
All
Eligibility Age
Minimum: 18 Years ~ Maximum: N/A
Countries
India
Locations

Postgraduate Institute of Medical Education and Research
Chandigarh, India

Postgraduate Institute of Medical Education and Research
NCT Number
Keywords
diffuse parenchymal lung disease
interstitial lung disease
organizing pneumonia
Coronavirus Disease-2019
SARS-Co-V-2
MeSH Terms
COVID-19
Lung Diseases
Prednisolone
Methylprednisolone Acetate
Methylprednisolone
Methylprednisolone Hemisuccinate
Prednisolone acetate
Prednisolone hemisuccinate
Prednisolone phosphate