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临床试验/NCT04338802
NCT04338802Unknown2 期

Efficacy and Safety of Nintedanib Ethanesulfonate Soft Capsule in the Treatment of Pulmonary Fibrosis in Patients With Moderate to Severe COVID-9(COVID 19) : a Single-center, Randomized, Placebo-controlled Study

Huilan Zhang0 个研究点目标入组 96 人开始时间: 2020年4月2日最近更新:
适应症
干预措施
相关药物

试验速览

阶段
2 期
发起方
入组人数
96
主要终点
Changes in forced vital capacity (FVC)

研究概览

简要总结

This center intends to conduct a single-center, randomized, placebo-controlled study to evaluate the effectiveness and safety of Nintedanib ethanesulfonate soft capsule in the treatment of pulmonary fibrosis in patients with moderate to severe COVID-19.

详细描述

This center intends to conduct a single-center, randomized, placebo-controlled study to evaluate the effectiveness and safety of Nintedanib ethanesulfonate soft capsule in the treatment of pulmonary fibrosis in patients with moderate to severe COVID-19. The number of cases is estimated based on the following:

This exploratory trial is expected to complete 80 case studies (randomly divided into control group and test group each with 40 cases), and the expected drop-out rate is not more than 20%, so the total number of cases is 96. Placebo control group:

Empty capsules with the same appearance and ingredients as Nintedanib soft capsules: one capsule at a time, twice a day, with an interval of about 12 hours each time. Continuous medication for 8 weeks.

Nintedanib Nintedanib cloth sulfonate soft capsule treatment: According to the drug manual recommendation, give Nintedanib cloth sulfonate soft capsule 150mg twice daily with an interval of about 12 hours each time, with food. Continuous medication for 8 weeks.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
主要目的
Treatment
盲法
None

入排标准

年龄范围
18 Years 至 70 Years(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • 18-70 years old (including 18 and 70 years old), regardless of gender;
  • Infection with new coronavirus pneumonia was confirmed by throat swab nucleic acid test. Patients with severe and critical illness were clinically judged. The symptoms of acute infection have been alleviated after treatment (at least 14 days after onset, no fever for more than 3 days), and the disease is recovering Within three months;
  • CT examination of patients with multiple fibrotic shadows in both lungs;
  • Blood routine, liver, and kidney functions are within the controllable range: such as the normal upper limit of plasma total bilirubin and creatinine ≤ 1.5 times; AST, ALT, LDH ≤ 2 times the normal upper limit; sufficient hematopoietic function: such as white blood cells ≥4.0 × 109 / L, platelets ≥100 × 109 / L;
  • Signed informed consent.

排除标准

  • Previous history of chronic bronchitis, emphysema, interstitial lung disease or pulmonary heart disease;
  • Combining with other serious diseases: such as those who have suffered myocardial infarction and uncontrollable diabetes within 6 months, and are considered unsuitable to participate in the trial;
  • People with active peptic ulcer;
  • Patients during pregnancy and lactation
  • Patients with mental illness or others who cannot cooperate effectively;
  • Researcher judges uncomfortable to participate in trial

研究组 & 干预措施

Placebo group

Placebo Comparator

Empty capsules with the same appearance and ingredients as Nintedanib soft capsules: one capsule at a time, twice a day, with an interval of about 12 hours each time. Continuous medication for 8 weeks.

干预措施: Placebo (Other)

Nintedanib group

Experimental

Nintedanib cloth sulfonate soft capsule treatment: According to the drug manual recommendation, give Nintedanib cloth sulfonate soft capsule 150mg twice daily with an interval of about 12 hours each time. Continuous medication for 8 weeks.

干预措施: Nintedanib 150 MG (Drug)

结局指标

主要结局

Changes in forced vital capacity (FVC)

时间窗: 8 weeks

Changes in forced vital capacity (FVC) after treatment compared to baseline.

次要结局

  • Changes in High resolution CT score(8 weeks)
  • Changes in carbon monoxide dispersion (DLco%)(8 weeks)
  • Changes in the six-minute walk test (6MWT)(8 weeks)

研究者

发起方
Huilan Zhang
申办方类型
Other
责任方
Sponsor Investigator
主要研究者

Huilan Zhang

Director of Respiratory and Critical Care Medicine , Tongji Hospital of Tongji Medical College, Huazhong University of Science and Technology

Tongji Hospital

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