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The clinic study in Fiberoptic Bronchoscopy With a Laryngeal Mask Airway

The clinic study in Fiberoptic Bronchoscopy With a Laryngeal Mask Airway

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR-TRC-13003692
Enrollment
Unknown
Registered
2013-07-13
Start date
2013-12-01
Completion date
Unknown
Last updated
2017-04-18

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

Conditions

The clinic study in Fiberoptic Bronchoscopy With a Laryngeal Mask Airway

Interventions

NLBM:bronchoscopy by mouth
NLBN:bronchoscopy by nose
LMA:bronchoscopy by nose

Sponsors

Department of thoracic surgery, Beijing Chao-Yang Hospital Affiliated China Capital Medical University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 75 Years

Inclusion criteria

Inclusion criteria: Patients were needed bronchoscopy biopsy in order to make clear the nature of the pulmonary diseases, who had no serious cardiovascular disease, and good heart lungs function. Before treatment the consent were informed and signed.

Exclusion criteria

Exclusion criteria: (1) The patients can not accept bronchoscopy due to the abnormal heart and lung function; (2) The patients had the history of throat diseases and can not received the laryngeal mask airway placement; (3)The bronchoscopy was performed without the need for biopsy.

Design outcomes

Primary

MeasureTime frame
the time of bronchoscopy just through subglottic;total operation time;the times of blood oxygen less than 80% so as to suspend procedure;

Countries

China

Contacts

Public ContactMiao Jinbai

Beijing chaoyang hospital affiliated China Capital Medical University

miaojinbai@163.com+86 13661127899

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 4, 2026