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Fibreoptic Bronchoscopy Assisted Intubation During Noninvasive Positive Pressure Ventilation

The Efficiency and Safety of Fibreoptic Bronchoscopy Assisted Intubation During Noninvasive Positive Pressure Ventilation

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT02462668
Acronym
FBAIDNIPPV
Enrollment
106
Registered
2015-06-04
Start date
2015-06-30
Completion date
2017-06-18
Last updated
2017-08-04

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

Conditions

Respiratory Failure

Keywords

Bronchoscopy, Intubation, Noninvasive positive pressure ventilation

Brief summary

This study is to investigate the efficiency and safety of fibreoptic bronchoscopy assisted intubation during noninvasive positive pressure ventilation in respiratory failure patients. Half of the participants will receive preoxygenation with noninvasive ventilator and fibreoptic bronchoscopy intubation during NIPPV. While the other half using usual preoxygenation(bag-mask ventilation ).

Detailed description

Respiratory failure is very common for critically ill patients, Main complication associated with intubation was desaturation. Usual preoxygenation( bag-mask ventilation) have been show that marginally effective in critically ill patients. As a result, there is a need to optimize the technique of preoxygenation to prolong the safe duration of apnea during the intubation procedure in critically ill patients. Noninvasive ventilation provides continuous positive airway pressure is effective in increasing the efficiency of gas exchange and in reducing the decrease in oxyhemoglobin saturation during fiberoptic bronchoscopy in hypoxemic patients. Therefore, our aim was to study whether NIPPV is more effective at reducing desaturation than usual preoxygenation in hypoxemic, critically ill patients requiring intubation in ICU.

Interventions

PROCEDUREBag-mask ventilation

The control group receives preoxygenation with bag-mask ventilation

PROCEDURENoninvasive positive pressure ventilation(NIPPV)

The NIPPV group receives noninvasive positive pressure ventilation during fibreoptic bronchoscopy assisted intubation

PROCEDUREfibreoptic bronchoscopy assisted intubation

All patients will receive fibreoptic bronchoscopy assisted intubation.

Sponsors

Lingbo Nong
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
SINGLE (Subject)

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* Acute respiratory failure requiring intubation, * Age greater than or equal to 18 years

Exclusion criteria

1. Nasal polyps,Nasopharyngeal cancer,Nasal bleeding,Rhinitis,Sinusitis and so on Nasal disease 2. Basal skull fracture 3. Severe coagulopathy, blood platelet counts \<50×10\*9/L 4. Nose and facial deformities, trauma 5. Cardiac arrest 6. Pregnancy or puerpera

Design outcomes

Primary

MeasureTime frame
Change in pulse oxymetry(SpO2)From time of randomization until connect to ventilator 30min

Secondary

MeasureTime frame
Mechanical ventilation Time28 days

Other

MeasureTime frame
28 days survival rateFrom the day of intubation to 28 days

Countries

China

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Mar 1, 2026