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Can bag-valve mask ventilation with positive end-expiratory pressure reduce hypoxia during intubation?A prospective, randomized, double-blind trial

Study on bag mask combined with end-expiratory positive pressure in patients with acute hypoxia

Status
Active, not recruiting
Phases
Early Phase 1
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2000035156
Enrollment
Unknown
Registered
2020-08-02
Start date
2020-08-10
Completion date
Unknown
Last updated
2020-08-03

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Acute respiratory failure

Interventions

experimental group:bag-valve mask ventilation with 10cmH2O positive end-expiratory pressure
control group:bag-valve mask ventilation

Sponsors

Peking Union Medical College Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 90 Years

Inclusion criteria

Inclusion criteria: 1. The patient is older than 18 years old; 2. Patients requiring endotracheal intubation in the ED for acute respiratory failure will be recruited. Acute respiratory failure is defined as a respiratory rate higher than 30/min, dyspnea at rest, a partial arterial oxygen pressure (PaO2) less than 60 mmHg on room air, or a PaO2 divided by the fraction of inspired oxygen (FiO2) less than 300 regardless of supplemental oxygen provided; 3. The patient and his/her family agree to have endotracheal intubation and sign the informed consent.

Exclusion criteria

Exclusion criteria: 1. Maternity; 2. Acute circulatory failure before intubation: hypotension requiring vasoactive drug therapy to maintain mean blood pressure over 65 mmHg; 3. Cardiac arrest before intubation; 4. Expected airway difficulty: the MACOCHA score was used to evaluate the airway as difficult; 5. The presence of right-to-left shunt heart disease and long-term hypoxia; 6. Difficulty in mask ventilation: insufficient mask sealing, excessive air leakage or excessive ventilation resistance; 7. Patients requiring urgent endotracheal intubation and difficulty in completing adequate preoxygenation time were assessed.

Design outcomes

Primary

MeasureTime frame
oxygen saturation;

Secondary

MeasureTime frame
blood pressure;Use of vasoactive medicine;Incidence of aspiration;

Countries

China

Contacts

Public ContactXujun

Peking Union Medical College Hospital

Xujunfree@126.com+86 15810578819

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 14, 2026