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Contact the study team using the details below to take part. If there are no contact details below please ask your doctor in the first instance.

Contact Information:

Dermot Linden, PhD 07812008626
dlinden02@qub.ac.uk


Danny McAuley, MD +442890 972144
d.f.mcauley@qub.ac.uk


Study Location:

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Be Part of Research - Trial Details - Hyperoxia Induced Pulmonary Inflammation and Organ Injury: a Human in Vivo Model

Hyperoxia Induced Pulmonary Inflammation and Organ Injury: a Human in Vivo Model

Recruiting

Open to: ALL

Age: 18.0 - 45.0

Medical Conditions

Pneumonia
Lung Injury
Acute Lung Injury
Inflammation
Hyperoxia
Wounds and Injuries


This information is provided directly by researchers, and we recognise that it isn't always easy to understand. We are working with researchers to improve the accessibility of this information. In some summaries, you may come across links to external websites. These websites will have more information to help you better understand the study.


Oxygen is the most commonly administered therapy in critical illness. Accumulating evidence suggests that patients often achieve supra-physiological levels of oxygenation in the critical care environment. Furthermore, hyperoxia related complications following cardiac arrest, myocardial infarction and stroke have also been reported. The underlying mechanisms of hyperoxia mediated injury remain poorly understood and there are currently no human in vivo studies exploring the relationship between hyperoxia and direct pulmonary injury and inflammation as well as distant organ injury.

The current trial is a mechanistic study designed to evaluate the effects of prolonged administration of high-flow oxygen (hyperoxia) on pulmonary and systemic inflammation. The study is a randomised, double-blind, placebo-controlled trial of high-flow nasal oxygen therapy versus matching placebo (synthetic medical air). We will also incorporate a model of acute lung injury induced by inhaled endotoxin (LPS) in healthy human volunteers. Healthy volunteers will undergo bronchoalveolar lavage (BAL) at 6 hours post-intervention to enable measurement of pulmonary and systemic markers of inflammation, oxidative stress and cellular injury.

Start dates may differ between countries and research sites. The research team are responsible for keeping the information up-to-date.  

The recruitment start and end dates are as follows:

Dec 2022 Dec 2024

INTERVENTIONAL

Intervention Type : DRUG
Intervention Description : Liquid medical oxygen will be administered for 6 hours using high-flow nasal cannula delivery system with an Fi02 of 100% and flow rate of 60 litres per minute.

Intervention Arm Group : Liquid medical oxygen;

Intervention Type : DRUG
Intervention Description : Synthetic medical air will be administered for 6 hours using high-flow nasal cannula delivery system with a flow rate of 60 litres per minute.

Intervention Arm Group : Synthetic medical air;



You can take part if:



You may not be able to take part if:


This is in the inclusion criteria above


Below are the locations for where you can take part in the trial. Please note that not all sites may be open.

  • Belfast Health and Social Care Trus
    Belfast


The study is sponsored by Belfast Health and Social Care Trust




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Read full details for Trial ID: NCT05414370
Last updated 26 January 2024

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