Comparison Between Different Ways for Using Lidocaine During FB

Not Applicable

Not yet recruiting

• Conditions: Lidocaine Spray; Nebulized Lidocaine; Lung Diseases; Lung Cancer

• Registration Number: NCT06563050
• Lead Sponsor: Assiut University

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Study Start: 2024-8-5
• Last Update Posted: 2 September 2024

Recruitment & Eligibility

• Status: Not yet recruiting
• Sex: All
• Target Recruitment: 240

Inclusion Criteria

Inclusion Criteria:<br><br> - Patients above 18 years old will undergo FB are included in this study.<br><br>Exclusion Criteria:<br><br> - known hypersensitivity to lidocaine.<br><br> - Pregnancy.<br><br> - hemodynamic instability.<br><br> - failure to provide informed consent.

Exclusion Criteria

Not provided

Study & Design

• Study Type: Interventional
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
The severity of cough using cough severity index;pain during the procedure rated by the subjects on the Faces Pain Rating Scale.;time taken to cross the vocal cords.;changes in heart rate;Changes in oxygen saturation

Secondary Outcome Measures

Name	Time	Method
cumulative dose of lidocaine administered during the procedure.;adverse reactions to lidocaine;overall satisfaction with the procedure using likert scale .