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Pre-hospital use of non-invasive ventilation improves acute respiratory failure

Completed
Conditions
Acute respiratory failure
Respiratory
Respiratory failure, not elsewhere classified
Registration Number
ISRCTN47620321
Lead Sponsor
Medical Service of the Bundeswehr (Sanitätsamt der Bundeswehr [SanABw]) (Germany)
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Completed
Sex
All
Target Recruitment
30
Inclusion Criteria

Pre-hospital patients:
1. Aged above 18 years, either sex
2. Acute dyspnoea
3. Respiratory rate greater than 25/min
4. Pulse oxymetric oxygen saturation less than 90%

Exclusion Criteria

1. Refusal of NIV
2. Vomiting
3. Glasgow Coma Scale less than 12 points
4. Suspected myocardial ischaemia
5. Systolic blood pressure less than 100 mmHg
6. Pregnancy
7. Injury of face or neck
8. Participation in another study

Study & Design

Study Type
Interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Rate of endotracheal intubation during first 24 hours of treatment.
Secondary Outcome Measures
NameTimeMethod
1. Difference of baseline and admission values of:<br>1.1. Pulse oxymetric oxygen saturation <br>1.2. Respiratory rate<br>1.3. Dyspnoea score<br>1.4. Heart rate<br>1.5. Systolic diastolic arterial blood pressure<br>2. Duration of intensive care<br>3. Incidence and duration of mechanical ventilation, and hospital days <br>4. Feasibility of NIV was rated at a scale from 1 to 5 (very good, good, acceptable, difficult, not feasible)
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