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Trial Documents & Resources

This page contains the current trial documentation including Current Protocol, Clinical Guidelines & Trial Materials. Please use your approved current localised forms for Patient Information Sheets (PIS) and Consent Forms

Trial Overview

How to deliver the intervention

UK NAVA is testing the effectiveness of neural drive monitoring and neurally-adjusted ventilatory assist.

PRINCIPLES

-The core intervention involves placing nasogastric tube into the patient safely.

-The specialised NGT is then connected to the ventilator and used to display the patient's neural drive which is otherwise invisible. This is used to establish whether a patient is breathing, how hard they are breathing, and how synchronised their breathing is to the current mode.

-Where possible the neural drive can then be used to trigger the pressure support breath, because in theory this should be more synchronised.

-If it is not possible to initiate or continue NAVA pressure support then we just need to know why.

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Inclusion criteria

  • Adult patients

  • Likely to remain ventilated > 48 hours from randomisation

  • Acute or chronic medical reason why weaning may be extended

Exclusion criteria

  • Unlikely to survive >24 hours

  • Receiving end-of-life care 

  • Contraindication to nasogastric or orogastric tube

  • Severe brain injury including brain-stem damage or hypoxic brain injury or requirement for neuroprotective ventilation

  • Spinal cord injury above C6 or phrenic nerve injury including Guillain Barre and Myaesthenia gravis

  • Home ventilation or referred/accepted for long-term ventilation unit care

  • Known/suspected portal hypertension

  • Temporary or permanent pacemaker

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Personal Legal Consent Video

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