Jet or Vibrating Mesh Nebulisation for Secretion Management in ICU
Respiratory Failure, Critical Illness
About this trial
This is an interventional treatment trial for Respiratory Failure focused on measuring nebuliser, secretions
Eligibility Criteria
Inclusion Criteria: Patient aged 18-80 years at time of recruitment to study Ventilated via an endotracheal tube or tracheostomy with an HME filter in the circuit Secretion load defined as patient requiring suctioning at least 2 times in the 6 hours prior to recruitment Sputum viscosity with grades 1 to 3 pourability in the Qualitative Sputum Assessment tool Not yet received saline nebulisation in the 6 hours prior to recruitment Likely to be ventilated via an endotracheal tube or tracheostomy for at least 3 days in the opinion of the treating clinician Exclusion Criteria: Pregnancy Pulmonary embolus Heart Failure (NYHA Grade III/IV) Clinical evidence of frank pulmonary oedema Cardiovascular instability (systolic BP ≤75 or heart rate ≥140)
Sites / Locations
- Queen Elizabeth University HospitalRecruiting
Arms of the Study
Arm 1
Arm 2
Arm 3
Experimental
Experimental
Active Comparator
Continuous nebulisation 0.9% saline Aerogen Solo vibrating mesh Nebuliser
Intermittent nebulisation 0.9% saline Aerogen Solo vibrating mesh Nebuliser
Intermittent standard nebulisation of 0.9% saline Intersurgical Cirrus 2 self sealing Jet Nebuliser
Continuous nebulization of 0.9% normal saline using the Aerogen Solo Nebuliser (50mls/24h continuous infusion using a syringe pump)
Intermittent nebulization of 0.9% normal saline using the Aerogen Solo Nebuliser (5mls 0.9% normal saline nebulised every 6 hours)
Intermittent standard nebulization of 0.9% normal saline using the Intersurgical Cirrus 2 self-sealing Jet Nebuliser ((5mls 0.9% normal saline nebulised every 6 hours)