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临床试验/NCT05648734
NCT05648734已完成不适用

Impact of Anti-Inflammatory and Anti-Fibrotic Drugs on Post-acute COVID-19 Pulmonary Fibrosis

Mansoura University1 个研究点 分布在 1 个国家目标入组 200 人开始时间: 2022年3月10日最近更新:
适应症
干预措施
相关药物

试验速览

阶段
不适用
状态
已完成
入组人数
200
试验地点
1
主要终点
Pulmonary Functions Test

研究概览

简要总结

In this study we aim to evaluate the radiological and functional changes in post-acute covid-19 pulmonary fibrosis patients in relation to anti-inflammatory and/or antifibrotic drugs prescribed during and after covid-19 pneumonia.

详细描述

This study is a prospective and retrospective cohort study in which post COVID-19 patients who are following up at post COVID-19 clinic are evaluated regarding presence and degree of Post COVID-19 Pulmonary Fibrosis (PCPF) in relation to anti-inflammatory and/or anti-fibrotic drugs.

Adult patients who have COVID-19 pneumonia confirmed either by RT-PCR or radiologically by CT scan and according to WHO severity classification are (Moderate, severe, or critical) and has received either:

  • Corticosteroids alone (≥ 20 mg prednisolone or its equivalent for ≥ 10 days after hospital discharge) - Group A.
  • Corticosteroids in combination with Colchicine (1 mg/day for ≥ 10 days) - Group B.
  • Corticosteroids in combination with Pirfenidone (267 mg TID for ≥ 14 days) - Group C.
  • Corticosteroids in combination with Colchicine and Pirfenidone (for ≥ 14 days) - Group D.

Pulmonary function test: Spirometry: measurement of lung volumes and capacities (forced expiratory volume in first second FEV1, Forced Vital Capacity FVC, FEV1/FVC and FEF25/75) after 1 month and 3 months of the onset of symptoms.

Radiological scoring: Baseline High resolution CT scan of the chest will be performed at baseline, 1 month and 3 months after onset of symptoms. Chest CT-Severity Scoring (Chest CT-SS) for assessing COVID-19 burden on the initial scan will be calculated. This score uses lung opacification as a surrogate for extension of the disease in the lungs. According to the anatomic structure, the 18 segments of both lungs were divided into 20 regions, in which the posterior apical segment of the left upper lobe was subdivided into apical and posterior segmental regions, whereas the anteromedial basal segment of the left lower lobe was subdivided into anterior and basal segmental regions. The lung opacities in all the 20 lung regions were subjectively evaluated on chest CT images using a system attributing score of 0, 1, and 2 if parenchymal opacification involved 0%, less than 50%, or equal to or more than 50% of each region, respectively. The CT-SS was defined as the sum of the individual scores in the 20 lung segment regions, which may range from 0 to 40 points

研究设计

研究类型
Observational
观察模型
Cohort
时间视角
Retrospective

入排标准

年龄范围
18 Years 至 —(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • Adult patients who have COVID-19 pneumonia confirmed either by RT-PCR or radiologically by CT scan and according to WHO severity classification are (Moderate, severe, or critical) and has received either: Corticosteroids alone.
  • Corticosteroids in combination with Colchicine.
  • Corticosteroids in combination with Pirfenidone.
  • Corticosteroids in combination with Colchicine and Pirfenidone.

排除标准

  • None COVID-19 pneumonia.
  • Patients with previous parenchymal lung disease.
  • Patients receiving anti-fibrotic or anti-inflammatory drugs due to other chronic disease.
  • Patients who received anti-fibrotic and or ant inflammatory drugs for duration and or doses less than presumed or those who reported noncompliance to treatment.
  • Patients with uncontrolled comorbidities.
  • Patients who develop severe intolerable side effects or derangement of liver enzymes more than 5 folds.
  • Pregnant ladies with COVID-19 pneumonia.

研究组 & 干预措施

Group A

Patients received Corticosteroids only

干预措施: Corticosteroids alone (Drug)

Group B

Patients received Corticosteroids in combination with Colchicine

干预措施: Corticosteroids + Colchicine (Drug)

Group C

Patients received Corticosteroids in combination with Pirfenidone

干预措施: Corticosteroids + Pirfenidone (Drug)

Group D

Patients received Corticosteroids in combination with Colchicine and Pirfenidone

干预措施: Corticosteroids + Colchicine + Pirfenidone for ≥ 14 days (Drug)

结局指标

主要结局

Pulmonary Functions Test

时间窗: 8 weeks

Change in FVC from 1 month to 3 months follow up after hospital discharge

Radiological scoring

时间窗: 8 weeks

Change in Chest CT Severity Scoring (Chest CT-SS) from 1 month to 3 months follow up after hospital discharge compared to baseline CT Chest scan

次要结局

未报告次要终点

研究者

申办方类型
Other
责任方
Sponsor

研究点 (1)

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