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Interventional Bronchoscopy Under Noninvasive Ventilation

Interventional Bronchoscopy Under Noninvasive Ventilation for Central Airway Stenosis

Status
UNKNOWN
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT02289586
Enrollment
40
Registered
2014-11-13
Start date
2014-07-31
Completion date
Unknown
Last updated
2014-11-13

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

Conditions

Central Airway Stenosis, Noninvasive Positive Pressure Ventilation;, Sedation;, Bronchoscopy;, Interventional;

Brief summary

To evaluate the effect and safety of noninvasive ventilation assisted interventional bronchoscopy for hypoxemia patients with central airway stenosis. With the sedation and analgesia, noninvasive ventilation assisted interventional bronchoscopy for hypoxemia patients with central airway stenosis is safe and effective, carries high satisfaction rate.

Interventions

DEVICEnoninvasive ventilation
DRUGsedation(dezocine and midazolam)
DRUGgeneral anesthesia(midazolam, fentanyl,rocuronium,propofol and Remifentanil)

Sponsors

Science and Technology Innovation Commission of Shenzhen Municipality
CollaboratorOTHER
Futian People's Hospital
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
NONE

Eligibility

Sex/Gender
ALL
Healthy volunteers
No

Inclusion criteria

* (a)patients with central airway stenosis need interventional bronchoscopy. (b) partial pressure of arterial oxygen (PaO2)/fraction of inspired oxygen (FiO2) ratio less than 300;

Exclusion criteria

* (a) facial deformity sufficient to preclude mask fitting; (b) upper gastrointestinal bleeding; (c) upper airway obstruction; (d) acute coronary syndromes; (e) tracheostomy or endotracheal intubation(ETI) before admission; (f) need for urgent ETI due to cardiac or respiratory arrest.

Design outcomes

Primary

MeasureTime frame
The improvement of airway stenosis after the operation1 day
The improvement of partial pressure of arterial oxygen (PaO2) after the operation1 day

Secondary

MeasureTime frame
hospitalization expensesDuring the period of hospitalization,an expected average of 4 weeks
hypoxemia during the operation1 day

Countries

China

Contacts

Primary ContactXiao-ke Chen, Master
007cxk@163.com+86-755-83982222

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026