Prospective randomized controlled trial on efficacy and safety by combined analgesics at sedative bronchoscopy using a BIS monitor
Not Applicable
- Conditions
- Peripheral lung lesion
- Registration Number
- JPRN-UMIN000032468
- Lead Sponsor
- Ehime University
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Complete: follow-up complete
- Sex
- All
- Target Recruitment
- 100
Inclusion Criteria
Not provided
Exclusion Criteria
1) History of severe drug allergy 2) Contraindications to use of midazolam and fentanyl 3) Using any opioids 4) Severe hypoxemia or hypercapnia 5) History of severe heart, lung, liver, kidney, neuromuscular disease 6) History of epilepsy 7) History of symptomatic cerebral infarction 8) During pregnancy or possible pregnancy 9) Emergency procedure 10) Bronchoscopy other than EBUS-GS 11) Other conditions inappropriate for participating in the study
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method The patient satisfaction score 2 hours after bronchoscopy using a visual analogue scale (VAS)
- Secondary Outcome Measures
Name Time Method