Last reviewed · How we verify
NCT05635903
Jet or Vibrating Mesh Nebulisation for Secretion Management in ICU
NA trial testing Continuous nebulisation 0.9% saline Aerogen Solo vibrating mesh Nebuliser in Respiratory Failure in 60 participants. Status unknown.
22 December 2023
Quick facts
| Lead sponsor | NHS Greater Glasgow and Clyde |
|---|---|
| Phase | NA |
| Status | Status unknown |
| Study type | INTERVENTIONAL |
| Allocation | randomized |
| Design | parallel |
| Masking | none |
| Primary purpose | treatment |
| Enrollment | 60 |
| Start date | 22 December 2019 |
| Primary completion | 22 December 2023 |
| Estimated completion | 22 December 2023 |
| Sites | 1 location across United Kingdom |
Drugs / interventions tested
- Continuous nebulisation 0.9% saline Aerogen Solo vibrating mesh Nebuliser
- Intermittent nebulisation 0.9% saline Aerogen vibrating mesh Solo Nebuliser
- Intermittent standard intermittent nebulisation of 0.9% saline Intersurgical Cirrus 2 self sealing Jet Nebuliser
Conditions studied
- Respiratory Failure — all drugs for Respiratory Failure →
- Critical Illness — all drugs for Critical Illness →
Sponsor
NHS Greater Glasgow and Clyde — full company profile →
Who can join
Adults 18 to 80, any sex, with Respiratory Failure or Critical Illness. Patients with the condition only — healthy volunteers not accepted.
Sponsor's own description
Critically unwell patients in Intensive Care have a decreased ability to effectively clear secretions. High secretion load is a major risk factor in the failure of tracheal extubation failure and the requirement for reintubation. Extubation failure is a predictor of poor outcome independent of the severity of the underlying illness. Nebulisation of isotonic saline can be employed to manage secretions by reducing the secretion viscosity and facilitating clearance of respiratory sections during tracheal suction. Standard jet nebulisers have been the mainstay of respiratory section management therapy in critical care since the early 1990s. A more recent development has been the vibrating mesh nebuliser. There is evidence of improved humidification and reduced water particle size and theoretically better transfer to the distal airways.
Publications & conference data
2 peer-reviewed publications reference this trial (live from Europe PMC):
-
Prospective randomised unblinded comparison of sputum viscosity for three methods of saline nebulisation in mechanically ventilated patients: A pilot study protocol.
Arnott A, Hart R, McQueen S, Watson M, et al · · 2023 · cited 3× · PMID 37590203 · DOI 10.1371/journal.pone.0290033 -
Prospective randomised unblinded comparison of sputum viscosity for three methods of saline nebulisation in mechanically ventilated patients: a study protocol
Arnott A, Hart R, McQueen S, Watson M, et al · · 2022 · DOI 10.21203/rs.3.rs-2346909/v1
Verify or expand the search:
- PubMed search for NCT05635903
- Europe PMC full search
- ASCO Meeting Library
- ESMO Meeting Library
- bioRxiv preprints
- medRxiv preprints
- Google Scholar
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Other NHS Greater Glasgow and Clyde trials
Trials by the same sponsor.
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Verify against primary sources
- ClinicalTrials.gov — authoritative US registry record
- WHO ICTRP — international registry index
- EU Clinical Trials Register
- Sponsor press releases (Google)
- Trial protocol + status: ClinicalTrials.gov NCT05635903 (US National Library of Medicine, public domain)
- Publications: Europe PMC API search by NCT ID, retrieved 10 June 2026
- Drug + disease cross-links: matched in real time against Drug Landscape's normalised drug + company + condition tables
- Sponsor: as reported to ClinicalTrials.gov by NHS Greater Glasgow and Clyde
- Last refreshed: 2 February 2023
Drug Landscape aggregates and links these public records for informational use only. Always verify against the primary source before clinical or regulatory decisions. Canonical URL: https://druglandscape.com/trial/NCT05635903.
Primary sources · FDA · ClinicalTrials.gov · EMA · SEC EDGAR · ChEMBL · Wikidata · full sourcing