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临床试验/NCT05184101
NCT05184101撤回2 期

INHALEd Nebulised Unfractionated HEParin for the Treatment of Hospitalised Patients With COVID-19 (INHALE-HEP) Australia

Australian National University1 个研究点 分布在 1 个国家开始时间: 2023年8月最近更新:
适应症
干预措施
相关药物

试验速览

阶段
2 期
状态
撤回
试验地点
1
主要终点
Intubation

研究概览

简要总结

Investigator-initiated, multi-centre, randomised, open-label trial of nebulised heparin sodium in addition to standard care compared to standard care alone in hospitalised patients with COVID-19 infection.

详细描述

Heparin has been used as a medicine for over 75 years. It is used mostly as an anticoagulant (blood thinner), injected under the skin or infused into a vein to prevent or treat large blood clots.

Most patients who are eligible for this study are already receiving heparin administered under the skin or into a vein, and this treatment would continue after enrolment in the study, as determined by the treating doctors according to best practice.

In this study heparin is administered using a nebuliser. A nebuliser is a device that changes a fluid into a mist of tiny droplets so it can be easily breathed into the lungs. A nebuliser is a commonly used and effective way of giving medications that work in the lungs. Nebulised heparin is not currently a standard treatment, but there are good reasons to think it could help.

Lung infections, including COVID-19, cause the widespread formation of tiny blood clots in the small blood vessels and air sacs of the lungs, which make breathing difficult and lead to lung damage. Previous studies of patients with serious breathing problems due to pneumonia and other conditions found that nebulised heparin reduced the formation of small blood clots in the lungs, reduced the amount of injury to the lungs and hastened recovery with faster return to living at home. The virus that causes COVID-19 (the SARS-CoV-2 virus) has 'spikes' on its surface that enable it to attach to cells of the body and enter those cells. Another way that nebulised heparin might help is by sticking to these spikes on the virus and inhibiting the ability of the virus to enter the cells.

The main aim is to determine if nebulised heparin reduces the chance that a patient needs help with their breathing from a mechanical ventilator. Other aims are to determine if nebulised heparin increases the chances of surviving and of getting better quicker.

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
Single (Outcomes Assessor)

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

  • Age 18 years or older
  • Currently admitted to hospital
  • There is a positive sample for COVID-19 within the past 14 days. The sample can be a nasal or pharyngeal swab, sputum, tracheal aspirate, bronchoalveolar lavage, or another sample from the patient
  • Requiring oxygenation according to the modified ordinal clinical scale 4-5

排除标准

  • Intubated and on mechanical ventilation, or requiring immediate intubation as per the treating clinician's assessment
  • Heparin allergy or heparin-induced thrombocytopaenia
  • Activated partial thromboplastin time (APTT) > 120 seconds, not due to anticoagulant therapy and does not correct with administration of fresh frozen plasma
  • Platelet count < 20 x 10^9 per L within 48 hours of randomisation
  • Pulmonary bleeding or uncontrolled bleeding within 48 hours of randomisation
  • Known or suspected pregnancy
  • Acute brain injury that may result in long-term disability
  • Myopathy, spinal cord injury, or nerve injury or disease with a likely prolonged incapacity to breathe independently e.g. Guillain-Barre syndrome
  • Treatment limitations in place, i.e. not for intubation, not for ICU admission
  • Death is imminent or inevitable within 24 hours
  • Clinician objection
  • Participant consent declined

研究组 & 干预措施

Nebulised heparin

Experimental

Participants assigned to 'nebulised heparin' will receive nebulised heparin in addition to the standard care required as determined by the treating team.

干预措施: Unfractionated Heparin (Drug)

结局指标

主要结局

Intubation

时间窗: 28 days

The primary outcome is intubation (or death, for patients who died before intubation) before or at day 28 after randomisation.

次要结局

  • Mortality(60 days)
  • Length of hospitalisation(60 days)
  • Oxygenation(28 days)

研究者

申办方类型
Other
责任方
Principal Investigator
主要研究者

Frank van Haren

Professor

Australian National University

研究点 (1)

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