Propofol versus midazolam/hydrocodone for sedation in flexible bronchoscopy: Safety and patient comfort - a non-inferiority trial

Completed

• Conditions: Sedation for flexible bronchoscopy; Respiratory

• Registration Number: ISRCTN99754241
• Lead Sponsor: niversity Hospital Basel (Switzerland)

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Study Start: 2008-02-14
• Last Update Posted: 13 January 2015

Recruitment & Eligibility

• Status: Completed
• Sex: All
• Target Recruitment: 200

Inclusion Criteria

1. Age >18 years
2. Need for flexible bronchoscopy

Exclusion Criteria

1. Invasive mechanical ventilation
2. Known allergy or intolerance to midazolam, hydrocodone or propofol
3. Inability to provide informed consent

Study & Design

• Study Type: Interventional
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
1. Mean lowest oxygen saturation during the procedure<br>2. Median patient overall well-being (comfort) at 1 hour after the procedure