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NCT07791992Withdrawn

Combination of High-flow Nasal Oxygen (Optiflow) and Vibrating Membrane Nebuliser (Aerogen) in the Pre-hospital Setting - Before/After Study

Source: ClinicalTrials.gov · Last updated 28 Aug 2026

Brief summary (registry, in English)

The aim of this observational before/after study is to determine how to optimally administer oxygen to patients experiencing an asthma or COPD exacerbation in emergency medical services. The aim will be to determine which method will achieve the target oxygen saturation objectives: \> 95% in asthma exacerbations and between 88% and 92% (or \> 92% in ambient air or with FiO2 21%) in COPD exacerbations. The study will compare a group "before" receiving standard care with a nebulizer mask to a group "after" using a combination of a vibrating membrane nebulizer and high-flow nasal oxygen.

Status (registry)
Withdrawn
Study type
Observational
Enrollment
0 (actual)
First submitted
28 Apr 2026
Start date
1 Oct 2026
Primary completion date
1 Oct 2027
Lead sponsor
Centre Hospitalier Sud Francilien
Diseases
Asthma
NCT number
NCT07791992

Who cannot take part

Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.

Other

  • Clinical signs of hypercapnia
  • Non French speaker
  • Contraindications to high-flow nasal oxygen: haemodynamic instability, Glasgow \< 12, cardiorespiratory arrest, lack of airway protection, cardiogenic pulmonary oedema
  • Indication for orotracheal intubation

Who the study is looking for

  • ≥ 18 years of age
  • Exacerbation of asthma or COPD requiring nebulization
  • Free and informed consent

Age in the registry: 18 years to - · Sex: All · Does not accept healthy volunteers

Full criteria on ClinicalTrials.gov

Sites (1)

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SiteCityCountrySite status
Centre Hospitalier Sud Francilien
Coordinator of this site? Confirm its status
Corbeil-EssonnesFranceUnknown status

This page is information, not medical advice. Discuss any trial with your doctor.