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Completed

NCT Number: NCT02462668

Fibreoptic Bronchoscopy Assisted Intubation During Noninvasive Positive Pressure Ventilation

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 ).

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Key information

Age range

18 year and older

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

The First Affiliated Hospital of Guangzhou Medical University

Guangzhou, Guangdong, 510120, China

About this study

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.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

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

Exclusion criteria

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

Treatment and study plan

Bag-mask ventilation

Procedure

The control group receives preoxygenation with bag-mask ventilation

Noninvasive positive pressure ventilation(NIPPV)

Procedure

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

fibreoptic bronchoscopy assisted intubation

Procedure

All patients will receive fibreoptic bronchoscopy assisted intubation.

Primary outcomes

  1. Change in pulse oxymetry(SpO2)

    Time frame: From time of randomization until connect to ventilator 30min

Secondary outcomes

  1. Mechanical ventilation Time

    Time frame: 28 days

Other outcomes

  1. 28 days survival rate

    Time frame: From the day of intubation to 28 days

Sponsors and collaborators

Lead sponsor

Lingbo Nong

Other

Registry information

Official study title

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

Acronym: FBAIDNIPPV

Important dates

Study start
2015
Primary completion
2017
Study completion
2017
First posted
Jun 4, 2015
Registry last updated
Aug 4, 2017

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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