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Comparison of flexible bronchoscope route between oral and nasal insertion on cough frequency.

Comparison of flexible bronchoscope route between oral and nasal insertion on cough frequency

Status
Unknown
Phases
Phase 4
Study type
Interventional
Source
TCTR
Registry ID
TCTR20240716009
Enrollment
77
Registered
2024-07-16
Start date
2023-12-01
Completion date
Unknown
Last updated
2026-08-03

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

Conditions

To compare cough frequency between oral versus nasal flexible bronchoscope route. cough frequency , oral, nasal, flexible bronchoscope

Interventions

Patients who go on flexible bronchoscope by oral rout insertion,Patients who go on flexible bronchoscope by nasal rout insertion
Experimental Device,Active Comparator Device
oral rout bronchoscope,nasal rout bronchoscope

Sponsors

Faculty of Medicine Vajira Hospital, Navamindradhiraj University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 80 Years

Inclusion criteria

Inclusion criteria: Patients over the age of 18 years old who had been go on flxible bronchoscope for bronchoalveolar lavage or transbronchial biopsy in the medicine department, Vajira Hospital, Navamindradhiraj University and had conditions follwing criteria : 1 patients who had inform consent 2 can communicated and assessed outcome after bronchoscope 3 stable vital sign before bronchoscope defined as heart rate less than 100 beats/min, blood pressure less than 150/90 mmHg

Exclusion criteria

Exclusion criteria: 1 Patients who go no bronchoscpoe with cryobiopsy 2 Baseline PaCO2 more than 45 mmHg 3. long term Oxygen therapy patients 4. have an upper airway obstruction or foreign body 5 current on antiplatelet or anticoagulant or withdrawal less than 5 days 6 Emergency bedside bronchoscope 7 Had head and neck surgery within 4 weeks 8 had a history of asthmatic attack, COPD with AE, or respiratory infection within 2 weeks 9 Had uncontroll allergic rhinitis or anomaly of head and neck

Design outcomes

Primary

MeasureTime frame
cough frequncy at intervention time cough frequency

Secondary

MeasureTime frame
time to vocal cord at intervention time time to vocal cord,total duration of procedure at intervention time total duration of procedure,dose of sedative drug at intervention time dose of sedative drug,comfortable score 48 hours after procedure comfortable score

Countries

Thailand

Contacts

Public ContactThamonwan Norasethasopon

Faculty of medicine Navamindradhiraj University

Thamonwan.n@nmu.ac.th0853534563

Outcome results

None listed

Source: TCTR (via WHO ICTRP) · Data processed: Aug 9, 2026